Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_004961.3 | 850 | Missense Mutation | GCC,GGC | A471G | NP_004952.2 |
XM_011531140.2 | 850 | Missense Mutation | GCC,GGC | A249G | XP_011529442.1 |
XM_017029386.1 | 850 | Missense Mutation | GCC,GGC | A358G | XP_016884875.1 |
XM_017029387.1 | 850 | Missense Mutation | GCC,GGC | A326G | XP_016884876.1 |
XM_017029388.1 | 850 | Missense Mutation | GCC,GGC | A278G | XP_016884877.1 |
XM_017029389.1 | 850 | UTR 3 | XP_016884878.1 |