Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001322340.1 | 2060 | Missense Mutation | ATC,GTC | I729V | NP_001309269.1 |
NM_001322341.1 | 2060 | Missense Mutation | ATC,GTC | I706V | NP_001309270.1 |
NM_001322342.1 | 2060 | Missense Mutation | ATC,GTC | I625V | NP_001309271.1 |
NM_001322343.1 | 2060 | Missense Mutation | ATC,GTC | I673V | NP_001309272.1 |
NM_001322344.1 | 2060 | Intron | NP_001309273.1 | ||
NM_022779.8 | 2060 | Missense Mutation | ATC,GTC | I802V | NP_073616.6 |
NM_138620.1 | 2060 | Intron | NP_619526.1 | ||
XM_005272207.4 | 2060 | Missense Mutation | ATC,GTC | I706V | XP_005272264.1 |
XM_006717236.3 | 2060 | UTR 3 | XP_006717299.1 | ||
XM_011518921.2 | 2060 | Intron | XP_011517223.1 | ||
XM_011518922.2 | 2060 | Intron | XP_011517224.1 |