| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_178170.2 | 572 | Missense Mutation | CAC,CTC | H123L | NP_835464.1 |
| XM_011524638.2 | 572 | Missense Mutation | CAC,CTC | H147L | XP_011522940.1 |
| XM_011524640.2 | 572 | Missense Mutation | CAC,CTC | H147L | XP_011522942.1 |
| XM_017024499.1 | 572 | Missense Mutation | CAC,CTC | H123L | XP_016879988.1 |
| XM_017024500.1 | 572 | Missense Mutation | CAC,CTC | H84L | XP_016879989.1 |
| XM_017024501.1 | 572 | Missense Mutation | CAC,CTC | H147L | XP_016879990.1 |