ENST00000232607.7:c.357T>C
MANE Select
|
ENSP00000232607.2:p.Cys119=
|
|
ENST00000232607.6:c.357T>C
|
ENSP00000232607.2:p.Cys119=
|
|
ENST00000460034.5:c.*101T>C
|
ENSP00000420409.1:n.*101T>C
|
|
ENST00000462091.5:c.*29T>C
|
ENSP00000417893.1:n.*29T>C
|
|
ENST00000467167.5:c.*255T>C
|
ENSP00000419618.1:n.*255T>C
|
|
ENST00000474588.5:c.311-301T>C
|
ENSP00000420348.1:n.311-301T>C
|
|
ENST00000479719.5:c.357T>C
|
ENSP00000420754.1:p.Cys119=
|
|
ENST00000497791.5:c.*29T>C
|
ENSP00000419121.1:n.*29T>C
|
|
ENST00000498715.1:n.75T>C
|
|
|
NM_000373.3:c.357T>C
|
NP_000364.1:p.Cys119=
|
|
NR_033434.1:n.309T>C
|
|
|
NR_033437.1:n.562T>C
|
|
|
XR_001740253.2:n.387T>C
|
|
|
NM_000373.4:c.357T>C
MANE Select
|
NP_000364.1:p.Cys119=
|
|
NR_033434.2:n.223T>C
|
|
|
NR_033437.2:n.476T>C
|
|
|