| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001278791.1 | 645 | Intron | NP_001265720.1 | ||
| NM_001278792.1 | 645 | Intron | NP_001265721.1 | ||
| NM_001278793.1 | 645 | Intron | NP_001265722.1 | ||
| NM_002914.4 | 645 | Intron | NP_002905.2 | ||
| NM_181471.2 | 645 | Intron | NP_852136.1 | ||
| XM_006716080.2 | 645 | Missense Mutation | ACT,ATT | T138I | XP_006716143.1 |
| XM_017012492.1 | 645 | Missense Mutation | ACT,ATT | T174I | XP_016867981.1 |
| XM_017012493.1 | 645 | Missense Mutation | ACT,ATT | T138I | XP_016867982.1 |