| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_032709.2 | 1778 | Missense Mutation | ATA,ATG | I563M | NP_116098.2 |
| XM_011540293.2 | 1778 | Missense Mutation | ATA,ATG | I597M | XP_011538595.1 |
| XM_011540301.2 | 1778 | Missense Mutation | ATA,ATG | I294M | XP_011538603.1 |
| XM_017016835.1 | 1778 | UTR 3 | XP_016872324.1 | ||
| XM_017016836.1 | 1778 | Intron | XP_016872325.1 | ||
| XM_017016837.1 | 1778 | Intron | XP_016872326.1 | ||
| XM_017016838.1 | 1778 | Missense Mutation | ATA,ATG | I442M | XP_016872327.1 |
| XM_017016839.1 | 1778 | Missense Mutation | ATA,ATG | I442M | XP_016872328.1 |
| XM_017016840.1 | 1778 | Missense Mutation | ATA,ATG | I442M | XP_016872329.1 |
| XM_017016841.1 | 1778 | Missense Mutation | ATA,ATG | I442M | XP_016872330.1 |