Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001144885.1 | 692 | Missense Mutation | CAC,CGC | H65R | NP_001138357.1 |
NM_001144886.1 | 692 | Missense Mutation | CAC,CGC | H39R | NP_001138358.1 |
NM_001144887.1 | 692 | Missense Mutation | CAC,CGC | H39R | NP_001138359.1 |
NM_004143.3 | 692 | Missense Mutation | CAC,CGC | H39R | NP_004134.2 |
XM_011530958.1 | 692 | Missense Mutation | CAC,CGC | H65R | XP_011529260.1 |