Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001039380.3 | 383 | Missense Mutation | GAT,GCT | D111A | NP_001034469.2 |
XM_017015895.1 | 383 | Missense Mutation | GAT,GCT | D111A | XP_016871384.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_006963.4 | 383 | Intron | NP_008894.2 |