Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_174937.3 | 1722 | Missense Mutation | AGC,GGC | S546G | NP_777597.2 |
XM_011539577.1 | 1722 | Missense Mutation | AGC,GGC | S559G | XP_011537879.1 |
XM_011539578.2 | 1722 | Intron | XP_011537880.1 |