| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001271680.1 | 380 | Intron | NP_001258609.1 | ||
| NM_021118.2 | 380 | Missense Mutation | CAT,CGT | H109R | NP_066941.1 |
| XM_005262086.3 | 380 | Missense Mutation | CAT,CGT | H108R | XP_005262143.1 |