| NM_004333.6:c.1855T>G
                    
                              MANE Select | NP_004324.2:p.Trp619Gly | 
            
              | ENST00000646891.2:c.1855T>G
                    
                        MANE Select | ENSP00000493543.1:p.Trp619Gly | 
            
              | NM_001374258.1:c.1975T>G
                    
                              MANE Plus Clinical | NP_001361187.1:p.Trp659Gly | 
            
              | ENST00000644969.2:c.1975T>G
                    
                        MANE Plus Clinical | ENSP00000496776.1:p.Trp659Gly | 
            
              | NM_001354609.1:c.1855T>G | NP_001341538.1:p.Trp619Gly | 
            
              | NM_001354609.2:c.1855T>G | NP_001341538.1:p.Trp619Gly | 
            
              | NM_001374244.1:c.1975T>G | NP_001361173.1:p.Trp659Gly | 
            
              | NM_001378467.1:c.1864T>G | NP_001365396.1:p.Trp622Gly | 
            
              | NM_001378468.1:c.1855T>G | NP_001365397.1:p.Trp619Gly | 
            
              | NM_001378469.1:c.1789T>G | NP_001365398.1:p.Trp597Gly | 
            
              | NM_001378470.1:c.1753T>G | NP_001365399.1:p.Trp585Gly | 
            
              | NM_001378471.1:c.1744T>G | NP_001365400.1:p.Trp582Gly | 
            
              | NM_001378472.1:c.1699T>G | NP_001365401.1:p.Trp567Gly | 
            
              | NM_001378473.1:c.1699T>G | NP_001365402.1:p.Trp567Gly | 
            
              | NM_001378474.1:c.1855T>G | NP_001365403.1:p.Trp619Gly | 
            
              | NM_001378475.1:c.1591T>G | NP_001365404.1:p.Trp531Gly | 
            
              | NM_004333.4:c.1855T>G , LRG_299t1:c.1855T>G | NP_004324.2:p.Trp619Gly | 
            
              | NM_004333.5:c.1855T>G | NP_004324.2:p.Trp619Gly | 
            
              | NR_148928.1:n.2953T>G |  | 
            
              | ENST00000288602.10:c.1855T>G | ENSP00000288602.6:p.Trp619Gly | 
            
              | ENST00000288602.11:c.1975T>G | ENSP00000288602.7:p.Trp659Gly | 
            
              | ENST00000479537.5:c.139T>G | ENSP00000418033.1:p.Trp47Gly | 
            
              | ENST00000479537.6:c.525T>G |  | 
            
              | ENST00000496384.6:c.678T>G |  | 
            
              | ENST00000496384.7:c.1855T>G | ENSP00000419060.2:p.Trp619Gly | 
            
              | ENST00000497784.1:c.1890T>G | ENSP00000420119.1:n.1890T>G | 
            
              | ENST00000497784.2:c.*1305T>G | ENSP00000420119.2:n.*1305T>G | 
            
              | ENST00000642228.1:c.*933T>G | ENSP00000493678.1:n.*933T>G | 
            
              | ENST00000642875.1:n.1259-3862T>G |  | 
            
              | ENST00000644120.1:n.2245T>G |  | 
            
              | ENST00000644650.1:c.951T>G |  | 
            
              | ENST00000644905.1:n.2737T>G |  | 
            
              | ENST00000646730.1:c.*431T>G | ENSP00000494784.1:n.*431T>G | 
            
              | ENST00000646891.1:c.1855T>G | ENSP00000493543.1:p.Trp619Gly | 
            
              | ENST00000647434.1:c.738-3862T>G | ENSP00000495132.1:n.738-3862T>G | 
            
              | XM_005250045.1:c.1855T>G | XP_005250102.1:p.Trp619Gly | 
            
              | XM_005250046.1:c.1855T>G | XP_005250103.1:p.Trp619Gly | 
            
              | XM_011516529.1:c.1855T>G | XP_011514831.1:p.Trp619Gly | 
            
              | XM_011516530.1:c.1695-3862T>G | XP_011514832.1:n.1695-3862T>G | 
            
              | XM_017012558.1:c.1975T>G | XP_016868047.1:p.Trp659Gly | 
            
              | XM_017012559.1:c.1975T>G | XP_016868048.1:p.Trp659Gly | 
            
              | XR_001744857.1:n.1983T>G |  | 
            
              | XR_001744858.1:n.1823-3862T>G |  | 
            
              | XR_242190.1:n.1863T>G |  | 
            
              | XR_927520.1:n.1863T>G |  | 
            
              | XR_927521.1:n.1863T>G |  | 
            
              | XR_927522.1:n.1703-3862T>G |  | 
            
              | XR_927523.1:n.1703-3862T>G |  |