Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_020693.3 | 4133 | Missense Mutation | CGG,TGG | R1952W | NP_065744.2 |
XM_011542917.1 | 4133 | Missense Mutation | CGG,TGG | R1904W | XP_011541219.1 |
XM_011542918.1 | 4133 | Missense Mutation | CGG,TGG | R1816W | XP_011541220.1 |
XM_011542919.2 | 4133 | Missense Mutation | CGG,TGG | R1465W | XP_011541221.1 |
XM_011542920.2 | 4133 | Missense Mutation | CGG,TGG | R1382W | XP_011541222.1 |
XM_011542921.2 | 4133 | Missense Mutation | CGG,TGG | R1183W | XP_011541223.1 |
XM_011542924.2 | 4133 | Missense Mutation | CGG,TGG | R1109W | XP_011541226.1 |
XM_011542925.2 | 4133 | Missense Mutation | CGG,TGG | R1103W | XP_011541227.1 |