Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001256599.1 | 1328 | Missense Mutation | CAT,CGT | H322R | NP_001243528.1 |
NM_001256600.1 | 1328 | Missense Mutation | CAT,CGT | H303R | NP_001243529.1 |
NM_001256601.1 | 1328 | Missense Mutation | CAT,CGT | H332R | NP_001243530.1 |
NM_001282378.1 | 1328 | Missense Mutation | CAT,CGT | H219R | NP_001269307.1 |
NM_001282379.1 | 1328 | Missense Mutation | CAT,CGT | H345R | NP_001269308.1 |
NM_025058.4 | 1328 | Missense Mutation | CAT,CGT | H345R | NP_079334.3 |
XM_011510002.1 | 1328 | Missense Mutation | CAT,CGT | H374R | XP_011508304.1 |
XM_017002393.1 | 1328 | Missense Mutation | CAT,CGT | H332R | XP_016857882.1 |