ENST00000698727.1:n.1598G>T
|
|
|
ENST00000698728.1:n.2117G>T
|
|
|
ENST00000698729.1:n.3663G>T
|
|
|
ENST00000698730.1:n.3663G>T
|
|
|
ENST00000698731.1:c.2397G>T
|
ENSP00000513898.1:p.Glu799Asp
|
|
ENST00000698732.1:c.*1399G>T
|
ENSP00000513899.1:n.*1399G>T
|
|
ENST00000698733.1:c.*1725G>T
|
ENSP00000513900.1:n.*1725G>T
|
|
ENST00000698734.1:c.2538G>T
|
ENSP00000513901.1:p.Glu846Asp
|
|
ENST00000698735.1:n.2653G>T
|
|
|
ENST00000698736.1:n.2653G>T
|
|
|
ENST00000698737.1:n.2653G>T
|
|
|
ENST00000698738.1:n.2653G>T
|
|
|
ENST00000698739.1:n.2653G>T
|
|
|
ENST00000372371.8:c.2538G>T
MANE Select
|
ENSP00000361446.3:p.Glu846Asp
|
|
ENST00000372371.7:c.2538G>T
|
ENSP00000361446.3:p.Glu846Asp
|
|
ENST00000472014.5:n.469+4657G>T
|
|
|
NM_007055.3:c.2538G>T
|
NP_008986.2:p.Glu846Asp
|
|
NM_007055.4:c.2538G>T
MANE Select
|
NP_008986.2:p.Glu846Asp
|
|