| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_016148.3 | 6126 | Missense Mutation | CAT,CGT | H2036R | NP_057232.2 |
| XM_006723233.3 | 6126 | Missense Mutation | CAT,CGT | H2036R | XP_006723296.1 |
| XM_011527013.2 | 6126 | Missense Mutation | CAT,CGT | H2044R | XP_011525315.1 |
| XM_011527014.2 | 6126 | Missense Mutation | CAT,CGT | H2027R | XP_011525316.1 |