Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_152326.2 | 1078 | Missense Mutation | CCG,CTG | P115L | NP_689539.1 |
XM_005267310.2 | 1078 | Missense Mutation | CCG,CTG | P115L | XP_005267367.1 |
XM_005267311.3 | 1078 | Missense Mutation | CCG,CTG | P115L | XP_005267368.1 |