ENST00000232607.7:c.525A>T
MANE Select
|
ENSP00000232607.2:p.Thr175=
|
|
ENST00000232607.6:c.525A>T
|
ENSP00000232607.2:p.Thr175=
|
|
ENST00000460034.5:c.*269A>T
|
ENSP00000420409.1:n.*269A>T
|
|
ENST00000462091.5:c.*197A>T
|
ENSP00000417893.1:n.*197A>T
|
|
ENST00000467167.5:c.*423A>T
|
ENSP00000419618.1:n.*423A>T
|
|
ENST00000474588.5:c.311-133A>T
|
ENSP00000420348.1:n.311-133A>T
|
|
ENST00000479719.5:c.525A>T
|
ENSP00000420754.1:p.Thr175=
|
|
ENST00000497791.5:c.*197A>T
|
ENSP00000419121.1:n.*197A>T
|
|
ENST00000498715.1:n.243A>T
|
|
|
NM_000373.3:c.525A>T
|
NP_000364.1:p.Thr175=
|
|
NR_033434.1:n.477A>T
|
|
|
NR_033437.1:n.730A>T
|
|
|
XR_001740253.2:n.555A>T
|
|
|
NM_000373.4:c.525A>T
MANE Select
|
NP_000364.1:p.Thr175=
|
|
NR_033434.2:n.391A>T
|
|
|
NR_033437.2:n.644A>T
|
|
|