| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001242791.1 | 342 | Missense Mutation | CAT,CGT | H62R | NP_001229720.1 |
| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001077503.1 | 342 | Intron | NP_001070971.1 | ||
| NM_001077504.1 | 342 | Intron | NP_001070972.1 | ||
| NM_001077505.1 | 342 | Intron | NP_001070973.1 | ||
| NM_001077506.1 | 342 | Intron | NP_001070974.1 | ||
| NM_170685.2 | 342 | Intron | NP_733786.2 |