| 
                  NM_004990.4:c.1795G>A
                    
                              MANE Select
                      
               | 
              
                  
                    NP_004981.2:p.Gly599Ser
                      
                  
               | 
            
            
              | 
                  ENST00000262027.10:c.1795G>A
                    
                        MANE Select
                      
               | 
              
                  
                    ENSP00000262027.5:p.Gly599Ser
                      
                  
               | 
            
            
              | 
                  NM_004990.3:c.1795G>A
               | 
              
                  
                    NP_004981.2:p.Gly599Ser
                      
                  
               | 
            
            
              | 
                  ENST00000262027.9:c.1795G>A
               | 
              
                  
                    ENSP00000262027.5:p.Gly599Ser
                      
                  
               | 
            
            
              | 
                  ENST00000537638.6:c.*87G>A
               | 
              
                  
                    ENSP00000446168.2:n.*87G>A
                  
               | 
            
            
              | 
                  ENST00000545888.6:c.*1296G>A
               | 
              
                  
                    ENSP00000439307.2:n.*1296G>A
                  
               | 
            
            
              | 
                  ENST00000546971.5:n.539G>A
               | 
              
                  
               | 
            
            
              | 
                  ENST00000548202.5:n.302G>A
               | 
              
                  
               | 
            
            
              | 
                  ENST00000548944.1:c.134-3703G>A
               | 
              
                  
                    ENSP00000449071.1:n.134-3703G>A
                  
               | 
            
            
              | 
                  ENST00000549048.1:n.460G>A
               | 
              
                  
               | 
            
            
              | 
                  ENST00000628866.2:c.*1296G>A
               | 
              
                  
                    ENSP00000486738.1:n.*1296G>A
                  
               | 
            
            
              | 
                  XM_006719398.2:c.1093G>A
               | 
              
                  
                    XP_006719461.1:p.Gly365Ser
                      
                  
               | 
            
            
              | 
                  XM_006719398.4:c.1093G>A
               | 
              
                  
                    XP_006719461.1:p.Gly365Ser
                      
                  
               | 
            
            
              | 
                  XM_011538353.1:c.*87G>A
               | 
              
                  
                    XP_011536655.1:n.*87G>A
                  
               | 
            
            
              | 
                  XR_001748704.2:n.1751G>A
               | 
              
                  
               | 
            
            
              | 
                  XR_002957327.1:n.1742G>A
               | 
              
                  
               |