Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001014436.2 | 771 | Intron | NP_001014436.1 | ||
NM_001122956.1 | 771 | Intron | NP_001116428.1 | ||
NM_001284313.1 | 771 | Intron | NP_001271242.1 | ||
NM_001284315.1 | 771 | Intron | NP_001271244.1 | ||
NM_014063.6 | 771 | Intron | NP_054782.2 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_000290.3 | 771 | Missense Mutation | ACG,ATG | T238M | NP_000281.2 |