| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001286157.1 | 1457 | Missense Mutation | ACT,GCT | T399A | NP_001273086.1 |
| NM_001323955.1 | 1457 | Missense Mutation | ACT,GCT | T437A | NP_001310884.1 |
| NM_006141.2 | 1457 | Missense Mutation | ACT,GCT | T476A | NP_006132.1 |
| XM_017023008.1 | 1457 | Intron | XP_016878497.1 |