Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001284511.1 | 677 | Intron | NP_001271440.1 | ||
NM_001284512.1 | 677 | Intron | NP_001271441.1 | ||
NM_001284513.1 | 677 | Missense Mutation | AGC,GGC | S16G | NP_001271442.1 |
NM_001324118.1 | 677 | Missense Mutation | AGC,GGC | S83G | NP_001311047.1 |
NM_152341.4 | 677 | Missense Mutation | AGC,GGC | S83G | NP_689554.2 |