| NM_001002295.2:c.778+1123T>C
                    
                              MANE Select | NP_001002295.1:n.778+1123T>C | 
            
              | ENST00000379328.9:c.778+1123T>C
                    
                        MANE Select | ENSP00000368632.3:n.778+1123T>C | 
            
              | NM_001002295.1:c.778+1123T>C | NP_001002295.1:n.778+1123T>C | 
            
              | NM_002051.2:c.778+1123T>C | NP_002042.1:n.778+1123T>C | 
            
              | NM_002051.3:c.778+1123T>C | NP_002042.1:n.778+1123T>C | 
            
              | ENST00000346208.3:c.778+1123T>C | ENSP00000341619.3:n.778+1123T>C | 
            
              | ENST00000346208.4:c.778+1123T>C | ENSP00000341619.3:n.778+1123T>C | 
            
              | ENST00000379328.7:c.778+1123T>C | ENSP00000368632.3:n.778+1123T>C | 
            
              | ENST00000461472.1:n.443+1123T>C |  | 
            
              | XM_005252442.2:c.778+1123T>C | XP_005252499.1:n.778+1123T>C | 
            
              | XM_005252443.3:c.778+1123T>C | XP_005252500.1:n.778+1123T>C | 
            
              | XM_005252443.5:c.778+1123T>C | XP_005252500.1:n.778+1123T>C |