Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001291812.1 | 551 | Intron | NP_001278741.1 | ||
NM_004464.3 | 551 | Missense Mutation | CCG,CTG | P105L | NP_004455.2 |
NM_033143.2 | 551 | Missense Mutation | CCG,CTG | P105L | NP_149134.1 |