| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001270614.1 | 766 | Silent Mutation | TGC,TGT | C207C | NP_001257543.1 |
| NM_001270615.1 | 766 | Silent Mutation | TGC,TGT | C202C | NP_001257544.1 |
| NM_133328.3 | 766 | Silent Mutation | TGC,TGT | C207C | NP_579874.1 |
| XM_011526569.1 | 766 | Silent Mutation | TGC,TGT | C247C | XP_011524871.1 |
| XM_011526571.1 | 766 | Missense Mutation | GCG,GTG | A240V | XP_011524873.1 |
| XM_011526572.1 | 766 | Nonsense Mutation | CGA,TGA | R215* | XP_011524874.1 |
| XM_017026402.1 | 766 | Silent Mutation | TGC,TGT | C247C | XP_016881891.1 |
| XM_017026403.1 | 766 | Missense Mutation | GCG,GTG | A268V | XP_016881892.1 |