Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_000298.5 | 1412 | Missense Mutation | CAC,CGC | H479R | NP_000289.1 |
NM_181871.3 | 1412 | Missense Mutation | CAC,CGC | H448R | NP_870986.1 |
XM_006711386.3 | 1412 | Missense Mutation | CAC,CGC | H415R | XP_006711449.1 |
XM_011509640.2 | 1412 | Missense Mutation | CAC,CGC | H415R | XP_011507942.1 |
XM_017001493.1 | 1412 | Intron | XP_016856982.1 |