Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001168215.1 | 393 | Missense Mutation | CGG,TGG | R95W | NP_001161687.1 |
NM_153229.2 | 393 | Missense Mutation | CGG,TGG | R95W | NP_694961.2 |
XM_006721730.3 | 393 | Missense Mutation | CGG,TGG | R95W | XP_006721793.1 |