| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_017629.3 | 569 | Missense Mutation | ACC,ATC | T165I | NP_060099.2 |
| XM_005270578.3 | 569 | Missense Mutation | ACC,ATC | T98I | XP_005270635.1 |
| XM_005270579.3 | 569 | Missense Mutation | ACC,ATC | T98I | XP_005270636.1 |
| XM_011540883.2 | 569 | Missense Mutation | ACC,ATC | T15I | XP_011539185.1 |
| XM_011540884.2 | 569 | Intron | XP_011539186.1 | ||
| XM_017000529.1 | 569 | Missense Mutation | ACC,ATC | T165I | XP_016856018.1 |