Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001198812.1 | 437 | Intron | NP_001185741.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_003692.4 | 437 | Missense Mutation | CCG,GCG | P44A | NP_003683.2 |