Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001176.3 | 149 | Intron | NP_001167.2 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_006849.2 | 149 | Missense Mutation | CCT,TCT | P33S | NP_006840.2 |