| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001001673.3 | 690 | Missense Mutation | CAT,CGT | H177R | NP_001001673.2 |
| NM_001110356.1 | 690 | Missense Mutation | CAT,CGT | H177R | NP_001103826.1 |
| NM_001110357.1 | 690 | Missense Mutation | CAT,CGT | H177R | NP_001103827.1 |
| NM_001110358.1 | 690 | Missense Mutation | CAT,CGT | H182R | NP_001103828.1 |
| NM_001110359.1 | 690 | Missense Mutation | CAT,CGT | H182R | NP_001103829.1 |
| NM_001110360.1 | 690 | Missense Mutation | CAT,CGT | H182R | NP_001103830.1 |
| NM_001110361.1 | 690 | Missense Mutation | CAT,CGT | H182R | NP_001103831.1 |
| NM_001289110.1 | 690 | Missense Mutation | CAT,CGT | H177R | NP_001276039.1 |