Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
XM_011528355.2 | 663 | Silent Mutation | TGC,TGT | C130C | XP_011526657.1 |
XM_011528356.2 | 663 | Intron | XP_011526658.1 | ||
XM_011528357.2 | 663 | Missense Mutation | GCG,GTG | A189V | XP_011526659.1 |