Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001098784.1 | 465 | Intron | NP_001092254.1 | ||
NM_001098785.1 | 465 | Intron | NP_001092255.1 | ||
NM_152832.2 | 465 | Intron | NP_690045.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001303024.1 | 465 | Silent Mutation | CCG,CCT | P76P | NP_001289953.1 |
NM_006396.2 | 465 | Silent Mutation | CCG,CCT | P113P | NP_006387.1 |