Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001123041.2 | 554 | Missense Mutation | CCG,CTG | P119L | NP_001116513.2 |
NM_001123396.1 | 554 | Missense Mutation | CCG,CTG | P119L | NP_001116868.1 |
XM_011534069.1 | 554 | Missense Mutation | CCG,CTG | P119L | XP_011532371.1 |