Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_013432.4 | 3661 | Missense Mutation | AGC,GGC | S1216G | NP_038460.4 |
XM_011517048.2 | 3661 | Missense Mutation | AGC,GGC | S892G | XP_011515350.1 |
XM_011517049.2 | 3661 | Missense Mutation | AGC,GGC | S880G | XP_011515351.1 |
XM_011517050.2 | 3661 | Intron | XP_011515352.1 |