| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001195833.1 | 1571 | Missense Mutation | CAC,CGC | H529R | NP_001182762.1 |
| NM_198445.3 | 1571 | Intron | NP_940847.1 | ||
| XM_006723015.2 | 1571 | Missense Mutation | CAC,CGC | H529R | XP_006723078.1 |
| XM_006723016.2 | 1571 | Missense Mutation | CAC,CGC | H415R | XP_006723079.1 |
| XM_011526454.2 | 1571 | Missense Mutation | CAC,CGC | H529R | XP_011524756.1 |
| XM_011526455.2 | 1571 | Missense Mutation | CAC,CGC | H497R | XP_011524757.1 |