Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001286725.1 | 882 | Missense Mutation | AGC,GGC | S30G | NP_001273654.1 |
NM_020866.2 | 882 | Missense Mutation | AGC,GGC | S30G | NP_065917.1 |
XM_017020678.1 | 882 | Intron | XP_016876167.1 | ||
XM_017020679.1 | 882 | Intron | XP_016876168.1 |