Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001098199.1 | 750 | Missense Mutation | CGG,TGG | R176W | NP_001091669.1 |
NM_001261452.1 | 750 | Missense Mutation | CGG,TGG | R176W | NP_001248381.1 |
NM_001261453.1 | 750 | Missense Mutation | CGG,TGG | R176W | NP_001248382.1 |
NM_001261454.1 | 750 | Missense Mutation | CGG,TGG | R176W | NP_001248383.1 |
NM_001261455.1 | 750 | Missense Mutation | CGG,TGG | R176W | NP_001248384.1 |
NM_005279.3 | 750 | Missense Mutation | CGG,TGG | R176W | NP_005270.2 |
XM_005246471.2 | 750 | Missense Mutation | CGG,TGG | R176W | XP_005246528.1 |
XM_017003832.1 | 750 | Missense Mutation | CGG,TGG | R176W | XP_016859321.1 |