Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001291284.1 | 1491 | Intron | NP_001278213.1 | ||
NM_007022.4 | 1491 | Intron | NP_008953.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_007024.4 | 1491 | Missense Mutation | CCG,CTG | P349L | NP_008955.1 |