Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001099791.2 | 887 | UTR 3 | NP_001093261.1 | ||
NM_001197129.1 | 887 | Intron | NP_001184058.1 | ||
NM_033542.3 | 887 | Intron | NP_291020.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_014477.2 | 887 | Nonsense Mutation | CGA,TGA | R183* | NP_055292.1 |
XM_011528790.2 | 887 | Nonsense Mutation | CGA,TGA | R167* | XP_011527092.1 |