| 
                  NM_002035.4:c.557A=
                    
                              MANE Select
                      
               | 
              
                  
                    NP_002026.1:p.Tyr186=
                  
               | 
            
            
              | 
                  ENST00000645214.2:c.557A=
                    
                        MANE Select
                      
               | 
              
                  
                    ENSP00000494352.1:p.Tyr186=
                  
               | 
            
            
              | 
                  NM_002035.2:c.557A=
               | 
              
                  
                    NP_002026.1:p.Tyr186=
                  
               | 
            
            
              | 
                  ENST00000326575.9:c.417+4264A=
               | 
              
                  
                    ENSP00000312939.5:n.417+4264A=
                  
               | 
            
            
              | 
                  ENST00000406396.7:c.557A=
               | 
              
                  
                    ENSP00000385083.2:p.Tyr186=
                  
               | 
            
            
              | 
                  ENST00000585750.1:n.251A=
               | 
              
                  
               | 
            
            
              | 
                  ENST00000591902.5:c.272A=
               | 
              
                  
                    ENSP00000468203.1:p.Tyr91=
                  
               | 
            
            
              | 
                  ENST00000591902.6:c.557A=
               | 
              
                  
                    ENSP00000468203.2:p.Tyr186=
                  
               | 
            
            
              | 
                  ENST00000644624.1:c.*496A=
               | 
              
                  
                    ENSP00000494878.1:n.*496A=
                  
               | 
            
            
              | 
                  ENST00000646205.1:c.*707A=
               | 
              
                  
                    ENSP00000496260.1:n.*707A=
                  
               | 
            
            
              | 
                  XM_005266677.1:c.557A=
               | 
              
                  
                    XP_005266734.1:p.Tyr186=
                  
               | 
            
            
              | 
                  XM_005266677.3:c.557A=
               | 
              
                  
                    XP_005266734.1:p.Tyr186=
                  
               | 
            
            
              | 
                  XM_006722433.2:c.470A=
               | 
              
                  
                    XP_006722496.1:p.Tyr157=
                  
               | 
            
            
              | 
                  XM_017025690.2:c.326A=
               | 
              
                  
                    XP_016881179.1:p.Tyr109=
                  
               |