Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001008393.3 | 373 | Missense Mutation | CCG,TCG | P42S | NP_001008394.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001281737.1 | 373 | Intron | NP_001268666.1 | ||
NM_001281738.1 | 373 | Intron | NP_001268667.1 | ||
NM_004453.3 | 373 | Intron | NP_004444.2 |