Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_020653.2 | 2732 | Missense Mutation | CAT,CGT | H760R | NP_065704.2 |
XM_011523968.2 | 2732 | Missense Mutation | CAT,CGT | H760R | XP_011522270.1 |
XM_017024887.1 | 2732 | Missense Mutation | CAT,CGT | H760R | XP_016880376.1 |