ENST00000698727.1:n.1285G>T
|
|
|
ENST00000698728.1:n.1804G>T
|
|
|
ENST00000698729.1:n.3350G>T
|
|
|
ENST00000698730.1:n.3350G>T
|
|
|
ENST00000698731.1:c.2084G>T
|
ENSP00000513898.1:p.Cys695Phe
|
|
ENST00000698732.1:c.*1086G>T
|
ENSP00000513899.1:n.*1086G>T
|
|
ENST00000698733.1:c.*1412G>T
|
ENSP00000513900.1:n.*1412G>T
|
|
ENST00000698734.1:c.2225G>T
|
ENSP00000513901.1:p.Cys742Phe
|
|
ENST00000698735.1:n.2340G>T
|
|
|
ENST00000698736.1:n.2340G>T
|
|
|
ENST00000698737.1:n.2340G>T
|
|
|
ENST00000698738.1:n.2340G>T
|
|
|
ENST00000698739.1:n.2340G>T
|
|
|
ENST00000372371.8:c.2225G>T
MANE Select
|
ENSP00000361446.3:p.Cys742Phe
|
|
ENST00000372371.7:c.2225G>T
|
ENSP00000361446.3:p.Cys742Phe
|
|
ENST00000472014.5:n.447G>T
|
|
|
ENST00000473588.2:c.888G>T
|
|
|
NM_007055.3:c.2225G>T
|
NP_008986.2:p.Cys742Phe
|
|
NM_007055.4:c.2225G>T
MANE Select
|
NP_008986.2:p.Cys742Phe
|
|