Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_014026.4 | 914 | Missense Mutation | TCC,TGC | S45C | NP_054745.1 |
XM_011542778.2 | 914 | Missense Mutation | TCC,TGC | S45C | XP_011541080.1 |
XM_011542780.2 | 914 | Intron | XP_011541082.1 | ||
XM_017017612.1 | 914 | UTR 5 | XP_016873101.1 |