|
ENST00000697194.1:c.1321G>A
(RHOT2)
|
ENSP00000513180.1:p.Gly441Ser
|
|
|
ENST00000315082.9:c.1318G>A
(RHOT2)
MANE Select
|
ENSP00000321971.4:p.Gly440Ser
|
|
|
ENST00000315082.8:c.1318G>A
(RHOT2)
|
ENSP00000321971.4:p.Gly440Ser
|
|
|
ENST00000561711.1:n.307G>A
(RHOT2)
|
|
|
|
ENST00000565004.5:n.571G>A
(RHOT2)
|
|
|
|
ENST00000568636.5:n.1800G>A
(RHOT2)
|
|
|
|
ENST00000569358.5:n.828G>A
(RHOT2)
|
|
|
|
ENST00000569675.5:n.1452G>A
(RHOT2)
|
|
|
|
ENST00000602564.5:n.2865G>A
(RHOT2)
|
|
|
|
ENST00000620831.4:c.-50+29073G>A
(MSLN)
|
ENSP00000482893.1:n.-50+29073G>A
|
|
|
NM_138769.2:c.1318G>A
(RHOT2)
|
NP_620124.1:p.Gly440Ser
|
|
|
XM_005255660.1:c.1321G>A
(RHOT2)
|
XP_005255717.1:p.Gly441Ser
|
|
|
XM_005255661.1:c.1267G>A
(RHOT2)
|
XP_005255718.1:p.Gly423Ser
|
|
|
XM_005255662.1:c.1264G>A
(RHOT2)
|
XP_005255719.1:p.Gly422Ser
|
|
|
XM_005255663.1:c.1219G>A
(RHOT2)
|
XP_005255720.1:p.Gly407Ser
|
|
|
XM_005255664.2:c.940G>A
(RHOT2)
|
XP_005255721.1:p.Gly314Ser
|
|
|
XM_006720970.1:c.1000G>A
(RHOT2)
|
XP_006721033.1:p.Gly334Ser
|
|
|
XM_006720971.1:c.1000G>A
(RHOT2)
|
XP_006721034.1:p.Gly334Ser
|
|
|
XM_006720973.1:c.898G>A
(RHOT2)
|
XP_006721036.1:p.Gly300Ser
|
|
|
XR_932964.1:n.1389G>A
(RHOT2)
|
|
|
|
NM_001352275.1:c.1321G>A
(RHOT2)
|
NP_001339204.1:p.Gly441Ser
|
|
|
NM_001352276.1:c.1267G>A
(RHOT2)
|
NP_001339205.1:p.Gly423Ser
|
|
|
NM_001352277.1:c.1264G>A
(RHOT2)
|
NP_001339206.1:p.Gly422Ser
|
|
|
NM_001352278.1:c.1219G>A
(RHOT2)
|
NP_001339207.1:p.Gly407Ser
|
|
|
NM_001352279.1:c.1165G>A
(RHOT2)
|
NP_001339208.1:p.Gly389Ser
|
|
|
NM_001352280.1:c.1000G>A
(RHOT2)
|
NP_001339209.1:p.Gly334Ser
|
|
|
NM_001352281.1:c.997G>A
(RHOT2)
|
NP_001339210.1:p.Gly333Ser
|
|
|
NM_001352282.1:c.997G>A
(RHOT2)
|
NP_001339211.1:p.Gly333Ser
|
|
|
NM_001352283.1:c.937G>A
(RHOT2)
|
NP_001339212.1:p.Gly313Ser
|
|
|
NM_001352284.1:c.901G>A
(RHOT2)
|
NP_001339213.1:p.Gly301Ser
|
|
|
NM_001352285.1:c.898G>A
(RHOT2)
|
NP_001339214.1:p.Gly300Ser
|
|
|
NM_001352286.1:c.841G>A
(RHOT2)
|
NP_001339215.1:p.Gly281Ser
|
|
|
NM_001352287.1:c.655G>A
(RHOT2)
|
NP_001339216.1:p.Gly219Ser
|
|
|
NM_001352288.1:c.655G>A
(RHOT2)
|
NP_001339217.1:p.Gly219Ser
|
|
|
NM_001352289.1:c.655G>A
(RHOT2)
|
NP_001339218.1:p.Gly219Ser
|
|
|
NM_001352290.1:c.655G>A
(RHOT2)
|
NP_001339219.1:p.Gly219Ser
|
|
|
NM_001352291.1:c.655G>A
(RHOT2)
|
NP_001339220.1:p.Gly219Ser
|
|
|
NM_001352292.1:c.655G>A
(RHOT2)
|
NP_001339221.1:p.Gly219Ser
|
|
|
NM_001352293.1:c.655G>A
(RHOT2)
|
NP_001339222.1:p.Gly219Ser
|
|
|
NM_001352294.1:c.655G>A
(RHOT2)
|
NP_001339223.1:p.Gly219Ser
|
|
|
NR_147953.1:n.1463G>A
(RHOT2)
|
|
|
|
NR_147954.1:n.1454G>A
(RHOT2)
|
|
|
|
NR_147955.1:n.1449G>A
(RHOT2)
|
|
|
|
NR_147956.1:n.1437G>A
(RHOT2)
|
|
|
|
XM_024450478.1:c.1834G>A
(RHOT2)
|
XP_024306246.1:p.Gly612Ser
|
|
|
XM_024450479.1:c.655G>A
(RHOT2)
|
XP_024306247.1:p.Gly219Ser
|
|
|
XM_024450480.1:c.655G>A
(RHOT2)
|
XP_024306248.1:p.Gly219Ser
|
|
|
XM_024450481.1:c.655G>A
(RHOT2)
|
XP_024306249.1:p.Gly219Ser
|
|
|
NM_138769.3:c.1318G>A
(RHOT2)
MANE Select
|
NP_620124.1:p.Gly440Ser
|
|
|
NM_001352275.2:c.1321G>A
(RHOT2)
|
NP_001339204.1:p.Gly441Ser
|
|
|
NM_001352276.2:c.1267G>A
(RHOT2)
|
NP_001339205.1:p.Gly423Ser
|
|
|
NM_001352277.2:c.1264G>A
(RHOT2)
|
NP_001339206.1:p.Gly422Ser
|
|
|
NM_001352278.2:c.1219G>A
(RHOT2)
|
NP_001339207.1:p.Gly407Ser
|
|
|
NM_001352279.2:c.1165G>A
(RHOT2)
|
NP_001339208.1:p.Gly389Ser
|
|
|
NM_001352280.2:c.1000G>A
(RHOT2)
|
NP_001339209.1:p.Gly334Ser
|
|
|
NM_001352281.2:c.997G>A
(RHOT2)
|
NP_001339210.1:p.Gly333Ser
|
|
|
NM_001352282.2:c.997G>A
(RHOT2)
|
NP_001339211.1:p.Gly333Ser
|
|
|
NM_001352283.2:c.937G>A
(RHOT2)
|
NP_001339212.1:p.Gly313Ser
|
|
|
NM_001352284.2:c.901G>A
(RHOT2)
|
NP_001339213.1:p.Gly301Ser
|
|
|
NM_001352285.2:c.898G>A
(RHOT2)
|
NP_001339214.1:p.Gly300Ser
|
|
|
NM_001352286.2:c.841G>A
(RHOT2)
|
NP_001339215.1:p.Gly281Ser
|
|
|
NM_001352288.2:c.655G>A
(RHOT2)
|
NP_001339217.1:p.Gly219Ser
|
|
|
NM_001352289.2:c.655G>A
(RHOT2)
|
NP_001339218.1:p.Gly219Ser
|
|
|
NM_001352290.2:c.655G>A
(RHOT2)
|
NP_001339219.1:p.Gly219Ser
|
|
|
NM_001352291.2:c.655G>A
(RHOT2)
|
NP_001339220.1:p.Gly219Ser
|
|
|
NM_001352292.2:c.655G>A
(RHOT2)
|
NP_001339221.1:p.Gly219Ser
|
|
|
NM_001352293.2:c.655G>A
(RHOT2)
|
NP_001339222.1:p.Gly219Ser
|
|
|
NM_001352294.2:c.655G>A
(RHOT2)
|
NP_001339223.1:p.Gly219Ser
|
|
|
NR_147953.2:n.1414G>A
(RHOT2)
|
|
|
|
NR_147954.2:n.1405G>A
(RHOT2)
|
|
|
|
NR_147955.2:n.1400G>A
(RHOT2)
|
|
|
|
NR_147956.2:n.1388G>A
(RHOT2)
|
|
|
