| NM_000749.5:c.-57G>C
                    
                              MANE Select | NP_000740.1:n.-57G>C | 
            
              | ENST00000289957.3:c.-57G>C
                    
                        MANE Select | ENSP00000289957.2:n.-57G>C | 
            
              | NM_000749.3:c.-57G>C | NP_000740.1:n.-57G>C | 
            
              | NM_000749.4:c.-57G>C | NP_000740.1:n.-57G>C | 
            
              | NM_001347717.1:c.-412G>C | NP_001334646.1:n.-412G>C | 
            
              | NM_001347717.2:c.-412G>C | NP_001334646.1:n.-412G>C | 
            
              | ENST00000289957.2:c.-57G>C | ENSP00000289957.2:n.-57G>C | 
            
              | ENST00000531610.5:n.115G>C |  | 
            
              | ENST00000534391.1:c.-412G>C | ENSP00000433913.1:n.-412G>C | 
            
              | XR_001745886.1:n.1622C>G |  | 
            
              | XR_001745887.1:n.552C>G |  | 
            
              | XR_949716.1:n.919C>G |  | 
            
              | XR_949717.1:n.1617C>G |  |