| 
                  NM_000428.3:c.4855C>G
                    
                              MANE Select
                      
               | 
              
                  
                    NP_000419.1:p.Gln1619Glu
                      
                  
               | 
            
            
              | 
                  ENST00000261978.9:c.4855C>G
                    
                        MANE Select
                      
               | 
              
                  
                    ENSP00000261978.4:p.Gln1619Glu
                      
                  
               | 
            
            
              | 
                  NM_000428.2:c.4855C>G
               | 
              
                  
                    NP_000419.1:p.Gln1619Glu
                      
                  
               | 
            
            
              | 
                  ENST00000261978.8:c.4855C>G
               | 
              
                  
                    ENSP00000261978.4:p.Gln1619Glu
                      
                  
               | 
            
            
              | 
                  ENST00000553939.5:c.4855C>G
               | 
              
                  
                    ENSP00000452110.1:p.Gln1619Glu
                      
                  
               | 
            
            
              | 
                  ENST00000556690.5:c.4723C>G
               | 
              
                  
                    ENSP00000451477.1:p.Gln1575Glu
                      
                  
               | 
            
            
              | 
                  XM_011536765.1:c.4474C>G
               | 
              
                  
                    XP_011535067.1:p.Gln1492Glu
                      
                  
               | 
            
            
              | 
                  XM_011536765.2:c.4474C>G
               | 
              
                  
                    XP_011535067.1:p.Gln1492Glu
                      
                  
               | 
            
            
              | 
                  XM_011536766.1:c.4396C>G
               | 
              
                  
                    XP_011535068.1:p.Gln1466Glu
                      
                  
               | 
            
            
              | 
                  XM_011536767.1:c.4372C>G
               | 
              
                  
                    XP_011535069.1:p.Gln1458Glu
                      
                  
               |