| NM_004525.3:c.12279C>T
                    
                              MANE Select | NP_004516.2:p.Pro4093= | 
            
              | ENST00000649046.1:c.12279C>T
                    
                        MANE Select | ENSP00000496870.1:p.Pro4093= | 
            
              | NM_004525.2:c.12279C>T | NP_004516.2:p.Pro4093= | 
            
              | ENST00000263816.7:c.12279C>T | ENSP00000263816.3:p.Pro4093= | 
            
              | ENST00000649153.1:c.3179C>T |  | 
            
              | ENST00000650252.1:c.1307C>T | ENSP00000496887.1:p.Pro436Leu | 
            
              | XM_011511183.1:c.12150C>T | XP_011509485.1:p.Pro4050= | 
            
              | XM_011511183.3:c.12150C>T | XP_011509485.1:p.Pro4050= | 
            
              | XM_011511184.1:c.9990C>T | XP_011509486.1:p.Pro3330= | 
            
              | XM_011511184.2:c.9990C>T | XP_011509486.1:p.Pro3330= |