The following pages link to Missense mutation
External toolsShowing 50 items.
View (previous 50 | next 50) (20 | 50 | 100 | 250 | 500)- Dravet syndrome (links | edit)
- Hypomagnesemia with secondary hypocalcemia (links | edit)
- Benign familial neonatal seizures (links | edit)
- Juvenile myoclonic epilepsy (links | edit)
- Catecholaminergic polymorphic ventricular tachycardia (links | edit)
- Estrogen insensitivity syndrome (links | edit)
- Ubiquitin-activating enzyme (links | edit)
- Sodium voltage-gated channel alpha subunit 9 (links | edit)
- Nuclear mitochondrial DNA segment (links | edit)
- Dynamic mutation (links | edit)
- Hay–Wells syndrome (links | edit)
- Keratin 5 (links | edit)
- Laminopathy (links | edit)
- P-type calcium channel (links | edit)
- CX3C motif chemokine receptor 1 (links | edit)
- 3-Hydroxy-3-methylglutaryl-CoA lyase (links | edit)
- Aldolase A deficiency (links | edit)
- Missense mRNA (links | edit)
- CHEK2 (links | edit)
- UTP—glucose-1-phosphate uridylyltransferase (links | edit)
- SLC22A5 (links | edit)
- D-bifunctional protein deficiency (links | edit)
- Helical growth (links | edit)
- Cornelia de Lange syndrome (links | edit)
- Fibroblast growth factor receptor 3 (links | edit)
- Anti-Müllerian hormone receptor (links | edit)
- ETV6 (links | edit)
- Steroidogenic factor 1 (links | edit)
- Dysfibrinogenemia (links | edit)
- Kuru (disease) (links | edit)
- Sodium/glucose cotransporter 1 (links | edit)
- Congenital myasthenic syndrome (links | edit)
- NPAS2 (links | edit)
- TRPA1 (links | edit)
- Retinol dehydrogenase (links | edit)
- RAB7A (links | edit)
- HIPK2 (links | edit)
- Methylated-DNA-protein-cysteine methyltransferase (links | edit)
- CLCN5 (links | edit)
- GABRB3 (links | edit)
- Hexokinase I (links | edit)
- MT-ATP6 (links | edit)
- Ribose-5-phosphate isomerase (links | edit)
- EPAS1 (links | edit)
- Collagen, type VII, alpha 1 (links | edit)
- RAPSN (links | edit)
- ACTC1 (links | edit)
- P4HB (links | edit)
- PSMB8 (links | edit)
- ADAR (links | edit)