Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_000374.4 | 471 | Missense Mutation | CGG,TGG | R122W | NP_000365.3 |
XM_005271169.1 | 471 | Missense Mutation | CGG,TGG | R50W | XP_005271226.1 |
XM_005271170.1 | 471 | Missense Mutation | CGG,TGG | R50W | XP_005271227.1 |