Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001198836.1 | 1089 | Intron | NP_001185765.1 | ||
NM_001198837.1 | 1089 | Intron | NP_001185766.1 | ||
NM_006328.3 | 1089 | Missense Mutation | TCC,TGC | S317C | NP_006319.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001198845.1 | 1089 | Intron | NP_001185774.1 | ||
NM_001198846.1 | 1089 | Intron | NP_001185775.1 |