ENST00000614874.2:c.*1138T>G
|
ENSP00000507272.1:n.*1138T>G
|
|
ENST00000682620.1:n.1761-952T>G
|
|
|
ENST00000684771.1:n.715-952T>G
|
|
|
ENST00000228872.9:c.*9-952T>G
MANE Select
|
ENSP00000228872.4:n.*9-952T>G
|
|
ENST00000228872.8:c.*9-952T>G
|
ENSP00000228872.4:n.*9-952T>G
|
|
ENST00000396340.1:c.476-981T>G
|
ENSP00000379629.1:n.476-981T>G
|
|
ENST00000442489.1:c.324-952T>G
|
ENSP00000407597.1:n.324-952T>G
|
|
ENST00000477087.1:n.285-952T>G
|
|
|
NM_004064.4:c.*9-952T>G
|
NP_004055.1:n.*9-952T>G
|
|
NM_004064.5:c.*9-952T>G
MANE Select
|
NP_004055.1:n.*9-952T>G
|
|