Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_015370.1 | 392 | Missense Mutation | CAC,CGC | H157R | NP_056185.1 |
XM_005261491.3 | 392 | Missense Mutation | CAC,CGC | H53R | XP_005261548.1 |
XM_011530096.2 | 392 | Missense Mutation | CAC,CGC | H116R | XP_011528398.1 |
XM_017028741.1 | 392 | Missense Mutation | CAC,CGC | H116R | XP_016884230.1 |