| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001277742.1 | 1307 | Missense Mutation | ACG,CCG | T427P | NP_001264671.1 |
| NM_019885.3 | 1307 | Missense Mutation | ACG,CCG | T502P | NP_063938.1 |
| XM_005264433.4 | 1307 | Missense Mutation | ACG,CCG | T444P | XP_005264490.1 |
| XM_011532988.1 | 1307 | Missense Mutation | ACG,CCG | T311P | XP_011531290.1 |