| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001281432.1 | 213 | Missense Mutation | CAT,CGT | H47R | NP_001268361.1 |
| NM_001281433.1 | 213 | Missense Mutation | CAT,CGT | H47R | NP_001268362.1 |
| NM_001281434.1 | 213 | Intron | NP_001268363.1 | ||
| NM_004773.3 | 213 | Missense Mutation | CAT,CGT | H47R | NP_004764.1 |