| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001039891.2 | 1693 | Missense Mutation | CAT,CGT | H432R | NP_001034980.1 |
| NM_001146291.1 | 1693 | Missense Mutation | CAT,CGT | H426R | NP_001139763.1 |
| NM_001190417.1 | 1693 | Missense Mutation | CAT,CGT | H427R | NP_001177346.1 |
| XM_011543941.2 | 1693 | Intron | XP_011542243.1 | ||
| XM_011543943.2 | 1693 | Intron | XP_011542245.1 | ||
| XM_011543944.2 | 1693 | Intron | XP_011542246.1 | ||
| XM_011543945.2 | 1693 | Intron | XP_011542247.1 | ||
| XM_017029728.1 | 1693 | Intron | XP_016885217.1 | ||
| XM_017029729.1 | 1693 | Intron | XP_016885218.1 | ||
| XM_017029730.1 | 1693 | Missense Mutation | CAT,CGT | H365R | XP_016885219.1 |
| XM_017029731.1 | 1693 | Intron | XP_016885220.1 | ||
| XM_017029732.1 | 1693 | Intron | XP_016885221.1 | ||
| XM_017029733.1 | 1693 | Intron | XP_016885222.1 |