Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001008901.1 | 573 | Missense Mutation | AAT,GAT | N89D | NP_001008901.1 |
NM_176791.3 | 573 | Missense Mutation | AAT,GAT | N89D | NP_789761.1 |
XM_005260298.4 | 573 | Intron | XP_005260355.1 |