Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_020812.3 | 5676 | Missense Mutation | CAC,CGC | H1861R | NP_065863.2 |
XM_005260000.2 | 5676 | Missense Mutation | CAC,CGC | H1927R | XP_005260057.1 |
XM_005260001.2 | 5676 | Missense Mutation | CAC,CGC | H1896R | XP_005260058.1 |
XM_006722804.3 | 5676 | Missense Mutation | CAC,CGC | H973R | XP_006722867.1 |
XM_011528150.1 | 5676 | Missense Mutation | CAC,CGC | H1907R | XP_011526452.1 |
XM_011528151.1 | 5676 | Missense Mutation | CAC,CGC | H1903R | XP_011526453.1 |
XM_011528152.1 | 5676 | Missense Mutation | CAC,CGC | H1872R | XP_011526454.1 |