Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_003906.4 | 6429 | Missense Mutation | CCA,CTA | P1950L | NP_003897.2 |
XM_005261203.4 | 6429 | Missense Mutation | CCA,CTA | P1950L | XP_005261260.1 |
XM_005261204.4 | 6429 | Missense Mutation | CCA,CTA | P1950L | XP_005261261.1 |
XM_005261205.3 | 6429 | Missense Mutation | CCA,CTA | P1950L | XP_005261262.1 |