Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001042663.1 | 2587 | Missense Mutation | TCC,TTC | S868F | NP_001036128.1 |
NM_001042664.1 | 2587 | Missense Mutation | TCC,TTC | S812F | NP_001036129.1 |
NM_001042665.1 | 2587 | Missense Mutation | TCC,TTC | S812F | NP_001036130.1 |
NM_001265592.1 | 2587 | Missense Mutation | TCC,TTC | S891F | NP_001252521.1 |
NM_001265593.1 | 2587 | Missense Mutation | TCC,TTC | S881F | NP_001252522.1 |
NM_001265594.1 | 2587 | Missense Mutation | TCC,TTC | S812F | NP_001252523.1 |
NM_020631.4 | 2587 | Missense Mutation | TCC,TTC | S812F | NP_065682.2 |
NM_198681.3 | 2587 | Missense Mutation | TCC,TTC | S889F | NP_941374.2 |