| NM_000020.3:c.1378-2A>T
                    
                              MANE Select | NP_000011.2:n.1378-2A>T | 
            
              | ENST00000388922.9:c.1378-2A>T
                    
                        MANE Select | ENSP00000373574.4:n.1378-2A>T | 
            
              | NM_000020.2:c.1378-2A>T , LRG_543t1:c.1378-2A>T | NP_000011.2:n.1378-2A>T | 
            
              | NM_001077401.1:c.1378-2A>T | NP_001070869.1:n.1378-2A>T | 
            
              | NM_001077401.2:c.1378-2A>T | NP_001070869.1:n.1378-2A>T | 
            
              | ENST00000388922.8:c.1378-2A>T | ENSP00000373574.4:n.1378-2A>T | 
            
              | ENST00000419526.6:c.856-2A>T | ENSP00000392492.2:n.856-2A>T | 
            
              | ENST00000547400.6:c.1108-2A>T | ENSP00000446724.2:n.1108-2A>T | 
            
              | ENST00000550683.5:c.1420-2A>T | ENSP00000447884.1:n.1420-2A>T | 
            
              | ENST00000551576.6:c.1378-2A>T | ENSP00000455848.2:n.1378-2A>T | 
            
              | XM_005269235.2:c.1378-2A>T | XP_005269292.1:n.1378-2A>T | 
            
              | XM_011539008.1:c.1108-2A>T | XP_011537310.1:n.1108-2A>T | 
            
              | XM_024449279.1:c.589-2A>T | XP_024305047.1:n.589-2A>T |