| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_015207.1 | 579 | Intron | NP_056022.1 | ||
| XM_005245792.3 | 579 | Missense Mutation | ACG,ATG | T1M | XP_005245849.1 |
| XM_005245793.3 | 579 | Missense Mutation | ACG,ATG | T1M | XP_005245850.1 |
| XM_005245794.3 | 579 | Intron | XP_005245851.1 |