Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001193511.1 | 2172 | Missense Mutation | GCC,GGC | A658G | NP_001180440.1 |
NM_006301.3 | 2172 | Missense Mutation | GCC,GGC | A625G | NP_006292.3 |
XM_005269138.3 | 2172 | Missense Mutation | GCC,GGC | A658G | XP_005269195.1 |
XM_005269140.2 | 2172 | Intron | XP_005269197.1 | ||
XM_006719588.3 | 2172 | Missense Mutation | GCC,GGC | A658G | XP_006719651.1 |
XM_011538725.2 | 2172 | Missense Mutation | GCC,GGC | A658G | XP_011537027.1 |
XM_017019956.1 | 2172 | Missense Mutation | GCC,GGC | A625G | XP_016875445.1 |