| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_000847.4 | 218 | Missense Mutation | CAT,GAT | H47D | NP_000838.3 |
| XM_006715072.3 | 218 | Intron | XP_006715135.1 | ||
| XM_011514533.2 | 218 | Intron | XP_011512835.1 | ||
| XM_017010794.1 | 218 | Intron | XP_016866283.1 |