| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_153252.4 | 5443 | Missense Mutation | CAT,CGT | H1727R | NP_694984.4 |
| XM_005262113.3 | 5443 | Missense Mutation | CAT,CGT | H1677R | XP_005262170.1 |
| XM_017029384.1 | 5443 | Missense Mutation | CAT,CGT | H1323R | XP_016884873.1 |
| XM_017029385.1 | 5443 | Intron | XP_016884874.1 |