| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001252675.1 | 1981 | Missense Mutation | CAT,CGT | H632R | NP_001239604.1 |
| NM_001252676.1 | 1981 | Missense Mutation | CAT,CGT | H513R | NP_001239605.1 |
| NM_001252677.1 | 1981 | Intron | NP_001239606.1 | ||
| NM_032501.3 | 1981 | Missense Mutation | CAT,CGT | H634R | NP_115890.2 |
| XM_006723659.1 | 1981 | Missense Mutation | CAT,CGT | H429R | XP_006723722.1 |
| XM_011529388.1 | 1981 | Missense Mutation | CAT,CGT | H416R | XP_011527690.1 |