| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001015885.1 | 477 | Missense Mutation | ACT,CCT | T38P | NP_001015885.1 |
| NM_003610.3 | 477 | Missense Mutation | ACT,CCT | T38P | NP_003601.1 |
| XM_005260582.2 | 477 | Missense Mutation | ACT,CCT | T38P | XP_005260639.2 |
| XM_005260583.2 | 477 | Missense Mutation | ACT,CCT | T76P | XP_005260640.1 |
| XM_011529087.2 | 477 | Missense Mutation | ACT,CCT | T38P | XP_011527389.1 |
| XM_011529088.2 | 477 | Missense Mutation | ACT,CCT | T38P | XP_011527390.1 |
| XM_011529089.1 | 477 | Missense Mutation | ACT,CCT | T38P | XP_011527391.1 |
| XM_017028108.1 | 477 | Missense Mutation | ACT,CCT | T38P | XP_016883597.1 |