Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_133637.2 | 1216 | Missense Mutation | CAC,CGC | H588R | NP_598376.2 |
XM_011532644.1 | 1216 | Missense Mutation | CAC,CGC | H470R | XP_011530946.1 |
XM_011532645.1 | 1216 | Missense Mutation | CAC,CGC | H346R | XP_011530947.1 |
XM_011532646.2 | 1216 | Intron | XP_011530948.1 | ||
XM_017003520.1 | 1216 | Missense Mutation | CAC,CGC | H256R | XP_016859009.1 |