Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001145536.1 | 1292 | Intron | NP_001139008.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_000080.3 | 1292 | Missense Mutation | CAC,CGC | H421R | NP_000071.1 |
XM_017024115.1 | 1292 | Missense Mutation | CAC,CGC | H409R | XP_016879604.1 |