Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001163424.1 | 1095 | Intron | NP_001156896.1 | ||
NM_138336.1 | 1095 | Missense Mutation | AGT,GGT | S224G | NP_612209.1 |
XM_017003411.1 | 1095 | Missense Mutation | AGT,GGT | S214G | XP_016858900.1 |