Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_052935.4 | 716 | Missense Mutation | TCT,TGT | S213C | NP_443167.4 |
XM_006721669.3 | 716 | Missense Mutation | TCT,TGT | S170C | XP_006721732.1 |
XM_006721670.3 | 716 | Missense Mutation | TCT,TGT | S170C | XP_006721733.1 |
XM_011524276.2 | 716 | Intron | XP_011522578.1 | ||
XM_011524277.2 | 716 | Intron | XP_011522579.1 | ||
XM_017024127.1 | 716 | Missense Mutation | CTG,GTG | L159V | XP_016879616.1 |