|
ENST00000273261.8:c.1614C>T
(LRIG1)
MANE Select
|
ENSP00000273261.3:p.Thr538=
|
|
|
ENST00000273261.7:c.1614C>T
(LRIG1)
|
ENSP00000273261.3:p.Thr538=
|
|
|
ENST00000383703.3:c.1686C>T
(LRIG1)
|
ENSP00000373208.3:p.Thr562=
|
|
|
ENST00000464350.6:c.*1548-28G>A
(SLC25A26)
|
ENSP00000432574.2:n.*1548-28G>A
|
|
|
ENST00000495037.1:n.630C>T
(LRIG1)
|
|
|
|
ENST00000496559.6:n.996C>T
(LRIG1)
|
|
|
|
NM_015541.2:c.1614C>T
(LRIG1)
|
NP_056356.2:p.Thr538=
|
|
|
XM_011533578.1:c.1470C>T
(LRIG1)
|
XP_011531880.1:p.Thr490=
|
|
|
XM_011533579.1:c.834C>T
(LRIG1)
|
XP_011531881.1:p.Thr278=
|
|
|
XM_011533578.2:c.1470C>T
(LRIG1)
|
XP_011531880.1:p.Thr490=
|
|
|
XM_011533579.3:c.834C>T
(LRIG1)
|
XP_011531881.1:p.Thr278=
|
|
|
XM_017006134.2:c.1539C>T
(LRIG1)
|
XP_016861623.1:p.Thr513=
|
|
|
XM_017006135.1:c.936C>T
(LRIG1)
|
XP_016861624.1:p.Thr312=
|
|
|
XM_017006136.2:c.834C>T
(LRIG1)
|
XP_016861625.1:p.Thr278=
|
|
|
NM_001377344.1:c.1539C>T
(LRIG1)
|
NP_001364273.1:p.Thr513=
|
|
|
NM_001377345.1:c.834C>T
(LRIG1)
|
NP_001364274.1:p.Thr278=
|
|
|
NM_001377346.1:c.834C>T
(LRIG1)
|
NP_001364275.1:p.Thr278=
|
|
|
NM_001377347.1:c.612C>T
(LRIG1)
|
NP_001364276.1:p.Thr204=
|
|
|
NM_001377348.1:c.585C>T
(LRIG1)
|
NP_001364277.1:p.Thr195=
|
|
|
NM_001377349.1:c.330C>T
(LRIG1)
|
NP_001364278.1:p.Thr110=
|
|
|
NM_015541.3:c.1614C>T
(LRIG1)
MANE Select
|
NP_056356.2:p.Thr538=
|
|
