| NM_005573.4:c.814-1G>T
                    
                              MANE Select | NP_005564.1:n.814-1G>T | 
            
              | ENST00000261366.10:c.814-1G>T
                    
                        MANE Select | ENSP00000261366.5:n.814-1G>T | 
            
              | NM_001198557.1:c.184-1G>T | NP_001185486.1:n.184-1G>T | 
            
              | NM_001198557.2:c.184-1G>T | NP_001185486.1:n.184-1G>T | 
            
              | NM_005573.3:c.814-1G>T | NP_005564.1:n.814-1G>T | 
            
              | NR_134488.1:n.1700-1G>T |  | 
            
              | ENST00000261366.9:c.814-1G>T | ENSP00000261366.5:n.814-1G>T | 
            
              | ENST00000395354.1:c.814-1G>T | ENSP00000378761.1:n.814-1G>T | 
            
              | ENST00000460265.5:c.814-1G>T | ENSP00000486528.1:n.814-1G>T | 
            
              | ENST00000472034.5:n.547-1G>T |  | 
            
              | ENST00000494185.1:n.60G>T |  | 
            
              | ENST00000504788.5:n.547-1G>T |  | 
            
              | XR_948250.1:n.1178-1G>T |  |