Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001271534.1 | 6438 | Missense Mutation | CGG,TGG | R1978W | NP_001258463.1 |
NM_001389.3 | 6438 | Missense Mutation | CGG,TGG | R1996W | NP_001380.2 |
XM_017028281.1 | 6438 | Missense Mutation | CGG,TGG | R1760W | XP_016883770.1 |