| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001024611.2 | 4099 | Missense Mutation | CAT,GAT | H789D | NP_001019782.1 |
| XM_011534383.2 | 4099 | Missense Mutation | CAT,GAT | H841D | XP_011532685.1 |
| XM_017008162.1 | 4099 | Missense Mutation | CAT,GAT | H553D | XP_016863651.1 |