| NM_001099287.2:c.453G>C
                  (NIPAL4)
                    
                              MANE Select | NP_001092757.2:p.Arg151Ser | 
            
              | ENST00000311946.8:c.453G>C
                  (NIPAL4)
                    
                        MANE Select | ENSP00000311687.8:p.Arg151Ser | 
            
              | NM_001099287.1:c.639G>C
                  (NIPAL4) | NP_001092757.1:p.Arg213Ser | 
            
              | NM_001172292.1:c.582G>C
                  (NIPAL4) | NP_001165763.1:p.Arg194Ser | 
            
              | ENST00000311946.7:c.639G>C
                  (NIPAL4) | ENSP00000311687.7:p.Arg213Ser | 
            
              | ENST00000435489.6:c.582G>C
                  (NIPAL4) | ENSP00000406456.2:p.Arg194Ser | 
            
              | ENST00000435489.7:c.396G>C
                  (NIPAL4) | ENSP00000406456.3:p.Arg132Ser | 
            
              | ENST00000517951.5:c.*1741+16581C>G
                  (ADAM19) | ENSP00000428376.1:n.*1741+16581C>G | 
            
              | ENST00000519150.1:c.551G>C
                  (NIPAL4) | ENSP00000430810.1:n.551G>C | 
            
              | XM_011534552.1:c.144G>C
                  (NIPAL4) | XP_011532854.1:p.Arg48Ser | 
            
              | XM_024446043.1:c.-61G>C
                  (NIPAL4) | XP_024301811.1:n.-61G>C |