Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001280558.1 | 461 | Missense Mutation | CAT,CCT | H124P | NP_001267487.1 |
NM_006032.3 | 461 | Missense Mutation | CAT,CCT | H69P | NP_006023.1 |
XM_005268216.1 | 461 | Missense Mutation | CAT,CCT | H69P | XP_005268273.1 |
XM_005268217.1 | 461 | UTR 5 | XP_005268274.1 |