Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_007202.3 | 2107 | Missense Mutation | AGT,GGT | S644G | NP_009133.2 |
XM_006721432.3 | 2107 | Missense Mutation | AGT,GGT | S586G | XP_006721495.1 |
XM_017024071.1 | 2107 | Intron | XP_016879560.1 |