| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001009813.2 | 1764 | Intron | NP_001009813.1 | ||
| NM_001301059.1 | 1764 | Intron | NP_001287988.1 | ||
| NM_020160.2 | 1764 | Intron | NP_064545.1 | ||
| XM_011527136.2 | 1764 | Missense Mutation | CAG,CAT | Q444H | XP_011525438.1 |
| XM_011527138.2 | 1764 | Missense Mutation | CAG,CAT | Q394H | XP_011525440.1 |
| XM_011527139.2 | 1764 | Intron | XP_011525441.1 | ||
| XM_011527140.1 | 1764 | Missense Mutation | CAG,CAT | Q241H | XP_011525442.1 |
| XM_017027011.1 | 1764 | Missense Mutation | CAG,CAT | Q461H | XP_016882500.1 |