| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001113525.1 | 464 | Missense Mutation | CAC,CGC | H126R | NP_001106997.1 |
| NM_152287.3 | 464 | Missense Mutation | CAC,CGC | H51R | NP_689500.2 |
| XM_005256324.3 | 464 | Missense Mutation | CAC,CGC | H126R | XP_005256381.1 |
| XM_005256328.3 | 464 | Intron | XP_005256385.1 | ||
| XM_017023889.1 | 464 | Missense Mutation | CAC,CGC | H126R | XP_016879378.1 |
| XM_017023890.1 | 464 | UTR 5 | XP_016879379.1 |