ENST00000232607.7:c.544A=
MANE Select
|
ENSP00000232607.2:p.Ile182=
|
|
ENST00000232607.6:c.544A=
|
ENSP00000232607.2:p.Ile182=
|
|
ENST00000460034.5:c.*288A=
|
ENSP00000420409.1:n.*288A=
|
|
ENST00000462091.5:c.*216A=
|
ENSP00000417893.1:n.*216A=
|
|
ENST00000467167.5:c.*442A=
|
ENSP00000419618.1:n.*442A=
|
|
ENST00000474588.5:c.311-114A=
|
ENSP00000420348.1:n.311-114A=
|
|
ENST00000479719.5:c.544A=
|
ENSP00000420754.1:p.Ile182=
|
|
ENST00000497791.5:c.*216A=
|
ENSP00000419121.1:n.*216A=
|
|
ENST00000498715.1:n.262A=
|
|
|
NM_000373.3:c.544A=
|
NP_000364.1:p.Ile182=
|
|
NR_033434.1:n.496A=
|
|
|
NR_033437.1:n.749A=
|
|
|
XR_001740253.2:n.574A=
|
|
|
NM_000373.4:c.544A=
MANE Select
|
NP_000364.1:p.Ile182=
|
|
NR_033434.2:n.410A=
|
|
|
NR_033437.2:n.663A=
|
|
|