|
NM_003119.4:c.1186G>T
MANE Select
|
NP_003110.1:p.Glu396Ter
|
|
ENST00000645818.2:c.1186G>T
MANE Select
|
ENSP00000495795.2:p.Glu396Ter
|
|
NM_001363850.1:c.1186G>T
|
NP_001350779.1:p.Glu396Ter
|
|
NM_003119.3:c.1186G>T
|
NP_003110.1:p.Glu396Ter
|
|
NM_199367.2:c.1186G>T
|
NP_955399.1:p.Glu396Ter
|
|
NM_199367.3:c.1186G>T
|
NP_955399.1:p.Glu396Ter
|
|
ENST00000268704.6:c.1186G>T
|
ENSP00000268704.2:p.Glu396Ter
|
|
ENST00000268704.7:c.1165G>T
|
ENSP00000268704.3:p.Glu389Ter
|
|
ENST00000341316.6:c.1186G>T
|
ENSP00000341157.2:p.Glu396Ter
|
|
ENST00000561945.1:n.230G>T
|
|
|
ENST00000561945.2:n.331G>T
|
|
|
ENST00000564409.1:n.645G>T
|
|
|
ENST00000564409.2:c.1242G>T
|
ENSP00000495297.1:n.1242G>T
|
|
ENST00000566682.2:c.199G>T
|
ENSP00000461979.2:p.Glu67Ter
|
|
ENST00000567138.2:c.68G>T
|
|
|
ENST00000567138.3:c.83G>T
|
|
|
ENST00000620811.4:c.-391G>T
|
ENSP00000478030.1:n.-391G>T
|
|
ENST00000642334.1:c.1059G>T
|
|
|
ENST00000642371.1:c.1265G>T
|
|
|
ENST00000642427.1:n.586G>T
|
|
|
ENST00000642436.1:n.389-8446G>T
|
|
|
ENST00000643105.1:c.1106G>T
|
|
|
ENST00000643307.1:c.1186G>T
|
ENSP00000495673.1:p.Glu396Ter
|
|
ENST00000643345.1:c.*710G>T
|
ENSP00000493982.1:n.*710G>T
|
|
ENST00000643370.1:c.360G>T
|
ENSP00000494895.1:p.Arg120Ser
|
|
ENST00000643496.1:n.1003G>T
|
|
|
ENST00000643649.1:c.1186G>T
|
ENSP00000494806.1:p.Glu396Ter
|
|
ENST00000643668.1:c.*1480G>T
|
ENSP00000494903.1:n.*1480G>T
|
|
ENST00000643724.1:c.*497+1690G>T
|
ENSP00000496335.1:n.*497+1690G>T
|
|
ENST00000643954.1:c.924G>T
|
|
|
ENST00000644171.1:n.1160G>T
|
|
|
ENST00000644210.1:c.1186G>T
|
ENSP00000495675.1:p.Glu396Ter
|
|
ENST00000644225.1:n.1203G>T
|
|
|
ENST00000644498.1:c.1165G>T
|
ENSP00000496244.1:p.Glu389Ter
|
|
ENST00000644671.1:c.843G>T
|
|
|
ENST00000644748.1:n.2617G>T
|
|
|
ENST00000644751.1:c.588G>T
|
|
|
ENST00000644781.1:c.1186G>T
|
ENSP00000495473.1:p.Glu396Ter
|
|
ENST00000644901.1:c.*1139G>T
|
ENSP00000493797.1:n.*1139G>T
|
|
ENST00000645042.1:c.1186G>T
|
ENSP00000493908.1:p.Glu396Ter
|
|
ENST00000645063.1:c.1186G>T
|
ENSP00000493590.1:p.Glu396Ter
|
|
ENST00000645258.1:c.117G>T
|
|
|
ENST00000645354.1:c.1946G>T
|
|
|
ENST00000645886.1:c.413G>T
|
|
|
ENST00000645897.1:c.987+1690G>T
|
ENSP00000495293.1:n.987+1690G>T
|
|
ENST00000645977.1:n.2304G>T
|
|
|
ENST00000646263.1:c.1186G>T
|
ENSP00000494119.1:p.Glu396Ter
|
|
ENST00000646303.1:c.1054G>T
|
ENSP00000494160.1:p.Glu352Ter
|
|
ENST00000646399.1:c.869G>T
|
|
|
ENST00000646445.1:c.183-12150G>T
|
|
|
ENST00000646454.1:n.710+1541G>T
|
|
|
ENST00000646531.1:c.1186G>T
|
ENSP00000495185.1:p.Glu396Ter
|
|
ENST00000646589.1:c.*314G>T
|
ENSP00000494739.1:n.*314G>T
|
|
ENST00000646716.1:c.377-12150G>T
|
ENSP00000495593.1:n.377-12150G>T
|
|
ENST00000646826.1:c.1186G>T
|
ENSP00000495123.1:p.Glu396Ter
|
|
ENST00000646930.1:c.1186G>T
|
ENSP00000495219.1:p.Glu396Ter
|
|
ENST00000646958.1:n.2231G>T
|
|
|
ENST00000647032.1:c.801G>T
|
|
|
ENST00000647079.1:c.778G>T
|
ENSP00000495967.1:p.Glu260Ter
|
|
ENST00000647227.1:c.949G>T
|
|
|
XM_005256321.3:c.1186G>T
|
XP_005256378.1:p.Glu396Ter
|
|
XM_005256321.4:c.1186G>T
|
XP_005256378.1:p.Glu396Ter
|
|
XM_006721264.2:c.1186G>T
|
XP_006721327.1:p.Glu396Ter
|
|
XM_006721264.4:c.1186G>T
|
XP_006721327.1:p.Glu396Ter
|
|
XM_011523306.1:c.1186G>T
|
XP_011521608.1:p.Glu396Ter
|
|
XM_011523307.1:c.1186G>T
|
XP_011521609.1:p.Glu396Ter
|
|
XM_017023597.1:c.1186G>T
|
XP_016879086.1:p.Glu396Ter
|
|
XM_017023598.1:c.1186G>T
|
XP_016879087.1:p.Glu396Ter
|
|
XR_001751971.2:n.1225G>T
|
|
|
XR_001751972.2:n.1225G>T
|
|
