Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001101662.1 | 3560 | Missense Mutation | AGT,TGT | S1080C | NP_001095132.1 |
NM_001242361.1 | 3560 | Missense Mutation | AGT,TGT | S1016C | NP_001229290.1 |
NM_002525.2 | 3560 | Missense Mutation | AGT,TGT | S1148C | NP_002516.2 |
XM_005270903.1 | 3560 | Missense Mutation | AGT,TGT | S843C | XP_005270960.1 |
XM_011541522.1 | 3560 | Missense Mutation | AGT,TGT | S1038C | XP_011539824.1 |
XM_011541523.1 | 3560 | Missense Mutation | AGT,TGT | S948C | XP_011539825.1 |
XM_011541525.2 | 3560 | Missense Mutation | AGT,TGT | S843C | XP_011539827.1 |
XM_017001375.1 | 3560 | Missense Mutation | AGT,TGT | S948C | XP_016856864.1 |