ENST00000232607.7:c.411G>A
MANE Select
|
ENSP00000232607.2:p.Glu137=
|
|
ENST00000232607.6:c.411G>A
|
ENSP00000232607.2:p.Glu137=
|
|
ENST00000460034.5:c.*155G>A
|
ENSP00000420409.1:n.*155G>A
|
|
ENST00000462091.5:c.*83G>A
|
ENSP00000417893.1:n.*83G>A
|
|
ENST00000467167.5:c.*309G>A
|
ENSP00000419618.1:n.*309G>A
|
|
ENST00000474588.5:c.311-247G>A
|
ENSP00000420348.1:n.311-247G>A
|
|
ENST00000479719.5:c.411G>A
|
ENSP00000420754.1:p.Glu137=
|
|
ENST00000497791.5:c.*83G>A
|
ENSP00000419121.1:n.*83G>A
|
|
ENST00000498715.1:n.129G>A
|
|
|
NM_000373.3:c.411G>A
|
NP_000364.1:p.Glu137=
|
|
NR_033434.1:n.363G>A
|
|
|
NR_033437.1:n.616G>A
|
|
|
XR_001740253.2:n.441G>A
|
|
|
NM_000373.4:c.411G>A
MANE Select
|
NP_000364.1:p.Glu137=
|
|
NR_033434.2:n.277G>A
|
|
|
NR_033437.2:n.530G>A
|
|
|