Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001304794.1 | 1287 | Missense Mutation | GAC,GTC | D182V | NP_001291723.1 |
NM_001304795.1 | 1287 | Missense Mutation | GAC,GTC | D182V | NP_001291724.1 |
NM_001304796.1 | 1287 | UTR 3 | NP_001291725.1 | ||
NM_152511.4 | 1287 | Missense Mutation | GAC,GTC | D182V | NP_689724.3 |
XM_005261368.4 | 1287 | Missense Mutation | GAC,GTC | D182V | XP_005261425.1 |
XM_006724148.3 | 1287 | Missense Mutation | GAC,GTC | D182V | XP_006724211.1 |
XM_011529920.2 | 1287 | Missense Mutation | GAC,GTC | D182V | XP_011528222.1 |
XM_011529921.2 | 1287 | Missense Mutation | GAC,GTC | D182V | XP_011528223.1 |
XM_017028627.1 | 1287 | Missense Mutation | GAC,GTC | D182V | XP_016884116.1 |
XM_017028628.1 | 1287 | Missense Mutation | GAC,GTC | D182V | XP_016884117.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001001479.3 | 1287 | Intron | NP_001001479.1 | ||
NM_001318370.1 | 1287 | Intron | NP_001305299.1 | ||
NM_001318371.1 | 1287 | Intron | NP_001305300.1 | ||
XM_017028794.1 | 1287 | Intron | XP_016884283.1 | ||
XM_017028795.1 | 1287 | Intron | XP_016884284.1 |