Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001278720.1 | 461 | Missense Mutation | GCC,GTC | A79V | NP_001265649.1 |
NM_001278721.1 | 461 | Intron | NP_001265650.1 | ||
NM_001318733.1 | 461 | Missense Mutation | GCC,GTC | A144V | NP_001305662.1 |
XM_017023849.1 | 461 | Missense Mutation | GCC,GTC | A144V | XP_016879338.1 |
XM_017023850.1 | 461 | Missense Mutation | GCC,GTC | A144V | XP_016879339.1 |