Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001321792.1 | 647 | Missense Mutation | CCG,CTG | P203L | NP_001308721.1 |
NM_013342.3 | 647 | Missense Mutation | CCG,CTG | P212L | NP_037474.1 |
XM_005278261.1 | 647 | Missense Mutation | CCG,CTG | P92L | XP_005278318.1 |