| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001258288.1 | 1681 | Missense Mutation | CAC,CGC | H398R | NP_001245217.1 |
| NM_001258289.1 | 1681 | Missense Mutation | CAC,CGC | H502R | NP_001245218.1 |
| NM_003944.3 | 1681 | Missense Mutation | CAC,CGC | H460R | NP_003935.2 |
| XM_017002757.1 | 1681 | Intron | XP_016858246.1 |