| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001032287.2 | 1635 | Intron | NP_001027458.1 | ||
| NM_001127362.1 | 1635 | Intron | NP_001120834.1 | ||
| NM_003297.3 | 1635 | Missense Mutation | ATG,ATT | M560I | NP_003288.2 |
| XM_005269133.2 | 1635 | Missense Mutation | ATG,ATT | M555I | XP_005269190.1 |
| XM_006719584.2 | 1635 | Missense Mutation | ATG,ATT | M514I | XP_006719647.1 |
| XM_006719585.2 | 1635 | Missense Mutation | ATG,ATT | M383I | XP_006719648.1 |
| XM_011538716.2 | 1635 | UTR 3 | XP_011537018.1 | ||
| XM_011538717.2 | 1635 | Missense Mutation | ATG,ATT | M464I | XP_011537019.1 |