Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_005103.4 | 689 | Intron | NP_005094.1 | ||
NM_022549.3 | 689 | Intron | NP_072043.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001301851.1 | 689 | Missense Mutation | CCT,GCT | P192A | NP_001288780.1 |