| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_152334.2 | 1657 | Missense Mutation | AGT,GGT | S718G | NP_689547.2 |
| XM_006720386.3 | 1657 | Silent Mutation | CCA,CCG | P693P | XP_006720449.1 |
| XM_017021912.1 | 1657 | Intron | XP_016877401.1 | ||
| XM_017021913.1 | 1657 | Missense Mutation | AGT,GGT | S475G | XP_016877402.1 |