| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001042537.1 | 114 | Missense Mutation | CAT,CGT | H13R | NP_001036002.1 |
| NM_001177651.1 | 114 | Intron | NP_001171122.1 | ||
| NM_006359.2 | 114 | Missense Mutation | CAT,CGT | H13R | NP_006350.1 |
| XM_006724726.3 | 114 | Intron | XP_006724789.1 | ||
| XM_011531243.2 | 114 | Intron | XP_011529545.1 | ||
| XM_017029223.1 | 114 | Intron | XP_016884712.1 | ||
| XM_017029224.1 | 114 | Intron | XP_016884713.1 | ||
| XM_017029225.1 | 114 | Intron | XP_016884714.1 |