| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001128602.1 | 2236 | Missense Mutation | CAT,CGT | H706R | NP_001122074.1 |
| NM_001306086.1 | 2236 | Intron | NP_001293015.1 | ||
| NM_005739.3 | 2236 | Missense Mutation | CAT,CGT | H741R | NP_005730.2 |
| XM_005254114.2 | 2236 | Missense Mutation | CAT,CGT | H690R | XP_005254171.1 |
| XM_011521151.2 | 2236 | Intron | XP_011519453.1 | ||
| XM_017021860.1 | 2236 | Missense Mutation | CAT,CGT | H693R | XP_016877349.1 |