Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001142389.1 | 642 | Missense Mutation | CCG,CTG | P192L | NP_001135861.1 |
NM_001172672.1 | 642 | Missense Mutation | CCG,CTG | P105L | NP_001166143.1 |
NM_004650.2 | 642 | Missense Mutation | CCG,CTG | P192L | NP_004641.1 |
XM_011545588.1 | 642 | Missense Mutation | CCG,CTG | P192L | XP_011543890.1 |