ENST00000265351.12:c.3222C>A
(XPO5)
MANE Select
|
ENSP00000265351.7:p.Thr1074=
|
|
ENST00000607635.2:c.922+3873G>T
(POLR1C)
|
ENSP00000496683.1:n.922+3873G>T
|
|
ENST00000643341.1:c.922+3873G>T
(POLR1C)
|
ENSP00000496018.1:n.922+3873G>T
|
|
ENST00000643799.1:c.*17+3604G>T
(POLR1C)
|
ENSP00000494529.1:n.*17+3604G>T
|
|
ENST00000646433.1:c.922+3873G>T
(POLR1C)
|
ENSP00000494368.1:n.922+3873G>T
|
|
ENST00000646700.1:c.922+3873G>T
(POLR1C)
|
ENSP00000495521.1:n.922+3873G>T
|
|
ENST00000265351.11:c.3222C>A
(XPO5)
|
ENSP00000265351.7:p.Thr1074=
|
|
ENST00000304004.7:c.922+3873G>T
(POLR1C)
|
ENSP00000307212.3:n.922+3873G>T
|
|
ENST00000455285.2:c.566C>A
(XPO5)
|
|
|
ENST00000455854.2:n.1705C>A
(XPO5)
|
|
|
ENST00000486936.2:c.409C>A
(XPO5)
|
|
|
ENST00000488195.6:n.619C>A
(XPO5)
|
|
|
NM_020750.2:c.3222C>A
(XPO5)
|
NP_065801.1:p.Thr1074=
|
|
XM_005249491.1:c.922+3873G>T
(POLR1C)
|
XP_005249548.1:n.922+3873G>T
|
|
XM_011515000.1:c.922+3873G>T
(POLR1C)
|
XP_011513302.1:n.922+3873G>T
|
|
NM_001318876.1:c.922+3873G>T
(POLR1C)
|
NP_001305805.1:n.922+3873G>T
|
|
NM_001363658.1:c.922+3873G>T
(POLR1C)
|
NP_001350587.1:n.922+3873G>T
|
|
NR_144392.1:n.3571C>A
(XPO5)
|
|
|
NM_020750.3:c.3222C>A
(XPO5)
MANE Select
|
NP_065801.1:p.Thr1074=
|
|
NM_001363658.2:c.922+3873G>T
(POLR1C)
|
NP_001350587.1:n.922+3873G>T
|
|
NM_001318876.2:c.922+3873G>T
(POLR1C)
|
NP_001305805.1:n.922+3873G>T
|
|
NR_144392.2:n.3534C>A
(XPO5)
|
|
|