ENST00000698727.1:n.1605T>C
|
|
|
ENST00000698728.1:n.2124T>C
|
|
|
ENST00000698729.1:n.3670T>C
|
|
|
ENST00000698730.1:n.3670T>C
|
|
|
ENST00000698731.1:c.2404T>C
|
ENSP00000513898.1:p.Phe802Leu
|
|
ENST00000698732.1:c.*1406T>C
|
ENSP00000513899.1:n.*1406T>C
|
|
ENST00000698733.1:c.*1732T>C
|
ENSP00000513900.1:n.*1732T>C
|
|
ENST00000698734.1:c.2545T>C
|
ENSP00000513901.1:p.Phe849Leu
|
|
ENST00000698735.1:n.2660T>C
|
|
|
ENST00000698736.1:n.2660T>C
|
|
|
ENST00000698737.1:n.2660T>C
|
|
|
ENST00000698738.1:n.2660T>C
|
|
|
ENST00000698739.1:n.2660T>C
|
|
|
ENST00000372371.8:c.2545T>C
MANE Select
|
ENSP00000361446.3:p.Phe849Leu
|
|
ENST00000372371.7:c.2545T>C
|
ENSP00000361446.3:p.Phe849Leu
|
|
ENST00000472014.5:n.469+4664T>C
|
|
|
NM_007055.3:c.2545T>C
|
NP_008986.2:p.Phe849Leu
|
|
NM_007055.4:c.2545T>C
MANE Select
|
NP_008986.2:p.Phe849Leu
|
|