| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001042729.1 | 1662 | Silent Mutation | CCA,CCG | P478P | NP_001036194.1 |
| NM_001042747.1 | 1662 | Silent Mutation | CCA,CCG | P478P | NP_001036212.1 |
| NM_005248.2 | 1662 | Silent Mutation | CCA,CCG | P478P | NP_005239.1 |
| XM_006710452.2 | 1662 | Silent Mutation | CCA,CCG | P478P | XP_006710515.1 |
| XM_011541010.1 | 1662 | Silent Mutation | CCA,CCG | P478P | XP_011539312.1 |
| XM_011541011.2 | 1662 | Silent Mutation | CCA,CCG | P409P | XP_011539313.1 |
| XM_011541012.1 | 1662 | UTR 3 | XP_011539314.1 | ||
| XM_011541013.2 | 1662 | Intron | XP_011539315.1 | ||
| XM_011541014.2 | 1662 | Silent Mutation | CCA,CCG | P274P | XP_011539316.1 |
| XM_017000673.1 | 1662 | Silent Mutation | CCA,CCG | P274P | XP_016856162.1 |
| XM_017000674.1 | 1662 | Silent Mutation | CCA,CCG | P274P | XP_016856163.1 |