| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001173473.1 | 1755 | Missense Mutation | CAC,CGC | H510R | NP_001166944.1 |
| NM_001173474.1 | 1755 | Missense Mutation | CAC,CGC | H552R | NP_001166945.1 |
| NM_004192.3 | 1755 | Missense Mutation | CAC,CGC | H568R | NP_004183.2 |
| XM_005274434.3 | 1755 | Missense Mutation | CAC,CGC | H568R | XP_005274491.1 |
| XM_011546185.2 | 1755 | Missense Mutation | CAC,CGC | H485R | XP_011544487.1 |
| XM_017029919.1 | 1755 | Missense Mutation | CAC,CGC | H459R | XP_016885408.1 |