Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_003782.3 | 1789 | Intron | NP_003773.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001164267.1 | 1789 | Missense Mutation | ACG,ATG | T519M | NP_001157739.1 |
NM_005452.5 | 1789 | Missense Mutation | ACG,ATG | T573M | NP_005443.3 |
XM_017011484.1 | 1789 | Missense Mutation | ACG,ATG | T573M | XP_016866973.1 |
XM_017011485.1 | 1789 | Missense Mutation | ACG,ATG | T251M | XP_016866974.1 |
XM_017011486.1 | 1789 | Missense Mutation | ACG,ATG | T229M | XP_016866975.1 |
XM_017011487.1 | 1789 | Missense Mutation | ACG,ATG | T229M | XP_016866976.1 |