ENST00000698727.1:n.1603T>C
|
|
|
ENST00000698728.1:n.2122T>C
|
|
|
ENST00000698729.1:n.3668T>C
|
|
|
ENST00000698730.1:n.3668T>C
|
|
|
ENST00000698731.1:c.2402T>C
|
ENSP00000513898.1:p.Phe801Ser
|
|
ENST00000698732.1:c.*1404T>C
|
ENSP00000513899.1:n.*1404T>C
|
|
ENST00000698733.1:c.*1730T>C
|
ENSP00000513900.1:n.*1730T>C
|
|
ENST00000698734.1:c.2543T>C
|
ENSP00000513901.1:p.Phe848Ser
|
|
ENST00000698735.1:n.2658T>C
|
|
|
ENST00000698736.1:n.2658T>C
|
|
|
ENST00000698737.1:n.2658T>C
|
|
|
ENST00000698738.1:n.2658T>C
|
|
|
ENST00000698739.1:n.2658T>C
|
|
|
ENST00000372371.8:c.2543T>C
MANE Select
|
ENSP00000361446.3:p.Phe848Ser
|
|
ENST00000372371.7:c.2543T>C
|
ENSP00000361446.3:p.Phe848Ser
|
|
ENST00000472014.5:n.469+4662T>C
|
|
|
NM_007055.3:c.2543T>C
|
NP_008986.2:p.Phe848Ser
|
|
NM_007055.4:c.2543T>C
MANE Select
|
NP_008986.2:p.Phe848Ser
|
|