Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001195833.1 | 728 | Missense Mutation | CCG,CTG | P216L | NP_001182762.1 |
NM_198445.3 | 728 | Intron | NP_940847.1 | ||
XM_006723015.2 | 728 | Missense Mutation | CCG,CTG | P216L | XP_006723078.1 |
XM_006723016.2 | 728 | Missense Mutation | CCG,CTG | P102L | XP_006723079.1 |
XM_011526454.2 | 728 | Missense Mutation | CCG,CTG | P216L | XP_011524756.1 |
XM_011526455.2 | 728 | Missense Mutation | CCG,CTG | P216L | XP_011524757.1 |