Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_207377.2 | 226 | Missense Mutation | AGC,GGC | S58G | NP_997260.1 |
XM_011536742.2 | 226 | Missense Mutation | AGC,GGC | S58G | XP_011535044.1 |
XM_011536743.2 | 226 | Missense Mutation | AGC,GGC | S58G | XP_011535045.1 |
XM_011536744.2 | 226 | Intron | XP_011535046.1 |