Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001085454.1 | 2363 | Missense Mutation | CGG,TGG | R726W | NP_001078923.1 |
NM_014030.3 | 2363 | Missense Mutation | CGG,TGG | R717W | NP_054749.2 |
XM_011524684.1 | 2363 | Missense Mutation | CGG,TGG | R733W | XP_011522986.1 |
XM_011524685.1 | 2363 | Missense Mutation | CGG,TGG | R724W | XP_011522987.1 |