Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001319674.1 | 384 | Intron | NP_001306603.1 | ||
NM_006582.3 | 384 | Missense Mutation | AAT,GAT | N47D | NP_006573.2 |
NM_024482.2 | 384 | Intron | NP_077808.1 | ||
XM_011540518.2 | 384 | Missense Mutation | AAT,GAT | N47D | XP_011538820.1 |
XM_011540519.2 | 384 | Missense Mutation | AAT,GAT | N47D | XP_011538821.1 |
XM_011540521.2 | 384 | Intron | XP_011538823.1 | ||
XM_011540522.2 | 384 | Intron | XP_011538824.1 | ||
XM_017000087.1 | 384 | Missense Mutation | AAT,GAT | N47D | XP_016855576.1 |