Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001098831.1 | 702 | Intron | NP_001092301.1 | ||
NM_178832.3 | 702 | Missense Mutation | CGG,TGG | R133W | NP_849154.1 |
XM_011539250.2 | 702 | Missense Mutation | CGG,TGG | R191W | XP_011537552.1 |
XM_011539251.2 | 702 | Missense Mutation | CGG,TGG | R133W | XP_011537553.1 |