| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001289174.1 | 2097 | Missense Mutation | CAT,CGT | H576R | NP_001276103.1 |
| NM_001289175.1 | 2097 | Missense Mutation | CAT,CGT | H518R | NP_001276104.1 |
| NM_001289176.1 | 2097 | Missense Mutation | CAT,CGT | H454R | NP_001276105.1 |
| NM_022553.5 | 2097 | Missense Mutation | CAT,CGT | H643R | NP_072047.4 |
| XM_011514797.1 | 2097 | Missense Mutation | CAT,CGT | H576R | XP_011513099.1 |
| XM_011514798.2 | 2097 | Missense Mutation | CAT,CGT | H576R | XP_011513100.1 |
| XM_011514799.1 | 2097 | Missense Mutation | CAT,CGT | H576R | XP_011513101.1 |
| XM_017011177.1 | 2097 | Intron | XP_016866666.1 | ||
| XM_017011178.1 | 2097 | Missense Mutation | CAT,CGT | H518R | XP_016866667.1 |
| XM_017011179.1 | 2097 | Intron | XP_016866668.1 |