Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001307980.1 | 482 | Missense Mutation | CCG,CGG | P20R | NP_001294909.1 |
NM_001307981.1 | 482 | Missense Mutation | CCG,CGG | P20R | NP_001294910.1 |
NM_005528.3 | 482 | Missense Mutation | CCG,CGG | P20R | NP_005519.2 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001128612.2 | 482 | Intron | NP_001122084.1 | ||
NM_001128613.2 | 482 | Intron | NP_001122085.1 | ||
NM_001271831.1 | 482 | Intron | NP_001258760.1 | ||
NM_032344.3 | 482 | Intron | NP_115720.1 |