Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_006295.2 | 3810 | Missense Mutation | CGG,TGG | R1131W | NP_006286.1 |
XM_005249362.2 | 3810 | Missense Mutation | CGG,TGG | R1132W | XP_005249419.1 |
XM_017011246.1 | 3810 | Missense Mutation | CGG,TGG | R549W | XP_016866735.1 |
XM_017011247.1 | 3810 | Missense Mutation | CGG,TGG | R549W | XP_016866736.1 |