Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001321449.1 | 635 | Missense Mutation | CCG,CTG | P183L | NP_001308378.1 |
NM_152358.2 | 635 | Missense Mutation | CCG,CTG | P183L | NP_689571.2 |
XM_011526436.2 | 635 | Silent Mutation | CCC,CCT | P173P | XP_011524738.1 |
XM_011526437.2 | 635 | Silent Mutation | CCC,CCT | P166P | XP_011524739.1 |