|
NM_000548.5:c.3598C>G
MANE Select
|
NP_000539.2:p.Arg1200Gly
|
|
ENST00000219476.9:c.3598C>G
MANE Select
|
ENSP00000219476.3:p.Arg1200Gly
|
|
NM_000548.3:c.3598C>G , LRG_487t1:c.3598C>G
|
NP_000539.2:p.Arg1200Gly
|
|
NM_000548.4:c.3598C>G
|
NP_000539.2:p.Arg1200Gly
|
|
NM_001077183.1:c.3466C>G
|
NP_001070651.1:p.Arg1156Gly
|
|
NM_001077183.2:c.3466C>G
|
NP_001070651.1:p.Arg1156Gly
|
|
NM_001077183.3:c.3466C>G
|
NP_001070651.1:p.Arg1156Gly
|
|
NM_001114382.1:c.3598C>G
|
NP_001107854.1:p.Arg1200Gly
|
|
NM_001114382.2:c.3598C>G
|
NP_001107854.1:p.Arg1200Gly
|
|
NM_001114382.3:c.3598C>G
|
NP_001107854.1:p.Arg1200Gly
|
|
NM_001318827.1:c.3358C>G
|
NP_001305756.1:p.Arg1120Gly
|
|
NM_001318827.2:c.3358C>G
|
NP_001305756.1:p.Arg1120Gly
|
|
NM_001318829.1:c.3322C>G
|
NP_001305758.1:p.Arg1108Gly
|
|
NM_001318829.2:c.3322C>G
|
NP_001305758.1:p.Arg1108Gly
|
|
NM_001318831.1:c.2866C>G
|
NP_001305760.1:p.Arg956Gly
|
|
NM_001318831.2:c.2866C>G
|
NP_001305760.1:p.Arg956Gly
|
|
NM_001318832.1:c.3499C>G
|
NP_001305761.1:p.Arg1167Gly
|
|
NM_001318832.2:c.3499C>G
|
NP_001305761.1:p.Arg1167Gly
|
|
NM_001363528.1:c.3469C>G
|
NP_001350457.1:p.Arg1157Gly
|
|
NM_001363528.2:c.3469C>G
|
NP_001350457.1:p.Arg1157Gly
|
|
NM_001370404.1:c.3466C>G
|
NP_001357333.1:p.Arg1156Gly
|
|
NM_001370405.1:c.3469C>G
|
NP_001357334.1:p.Arg1157Gly
|
|
NM_021055.2:c.3469C>G
|
NP_066399.2:p.Arg1157Gly
|
|
NM_021055.3:c.3469C>G
|
NP_066399.2:p.Arg1157Gly
|
|
ENST00000219476.7:c.3598C>G
|
ENSP00000219476.3:p.Arg1200Gly
|
|
ENST00000350773.8:c.3598C>G
|
ENSP00000344383.4:p.Arg1200Gly
|
|
ENST00000350773.9:c.3598C>G
|
ENSP00000344383.4:p.Arg1200Gly
|
|
ENST00000382538.10:c.3322C>G
|
ENSP00000371978.6:p.Arg1108Gly
|
|
ENST00000401874.6:c.3466C>G
|
ENSP00000384468.2:p.Arg1156Gly
|
|
ENST00000401874.7:c.3466C>G
|
ENSP00000384468.2:p.Arg1156Gly
|
|
ENST00000439117.6:c.*2765C>G
|
ENSP00000406980.2:n.*2765C>G
|
|
ENST00000439673.6:c.3358C>G
|
ENSP00000399232.2:p.Arg1120Gly
|
|
ENST00000497886.5:n.1425C>G
|
|
|
ENST00000568454.5:c.3499C>G
|
ENSP00000454487.1:p.Arg1167Gly
|
|
ENST00000568454.6:c.3499C>G
|
ENSP00000454487.1:p.Arg1167Gly
|
|
ENST00000568566.6:c.*2016C>G
|
ENSP00000455997.2:n.*2016C>G
|
|
ENST00000642206.2:c.3514C>G
|
ENSP00000495146.2:p.Arg1172Gly
|
|
ENST00000642365.1:c.2252C>G
|
|
|
ENST00000642365.2:c.3595C>G
|
ENSP00000495459.2:p.Arg1199Gly
|
|
ENST00000642561.1:c.3469C>G
|
ENSP00000495099.1:p.Arg1157Gly
|
|
ENST00000642797.1:c.3469C>G
|
ENSP00000493846.1:p.Arg1157Gly
|
|
ENST00000642936.1:c.3466C>G
|
ENSP00000494514.1:p.Arg1156Gly
|
|
ENST00000643088.1:c.3466C>G
|
ENSP00000494747.1:p.Arg1156Gly
|
|
ENST00000643426.1:n.29C>G
|
|
|
ENST00000643946.1:c.3598C>G
|
ENSP00000495927.1:p.Arg1200Gly
|
|
ENST00000644043.1:c.3469C>G
|
ENSP00000496262.1:p.Arg1157Gly
|
|
ENST00000644329.1:c.3466C>G
|
ENSP00000496611.1:p.Arg1156Gly
|
|
ENST00000644335.1:c.3469C>G
|
ENSP00000496317.1:p.Arg1157Gly
|
|
ENST00000644399.1:c.3588C>G
|
|
|
ENST00000644417.2:c.*4047C>G
|
ENSP00000493912.2:n.*4047C>G
|
|
ENST00000644722.1:n.744C>G
|
|
|
ENST00000645024.1:n.1751C>G
|
|
|
ENST00000646388.1:c.3598C>G
|
ENSP00000495921.1:p.Arg1200Gly
|
|
ENST00000646464.2:c.*4520C>G
|
ENSP00000496610.2:n.*4520C>G
|
|
ENST00000646634.1:n.2482C>G
|
|
|
ENST00000646674.1:n.213C>G
|
|
|
ENST00000647042.1:n.890C>G
|
|
|
ENST00000647180.1:n.78C>G
|
|
|
XM_005255529.3:c.3469C>G
|
XP_005255586.2:p.Arg1157Gly
|
|
XM_005255531.3:c.3469C>G
|
XP_005255588.2:p.Arg1157Gly
|
|
XM_005255531.4:c.3469C>G
|
XP_005255588.2:p.Arg1157Gly
|
|
XM_011522636.1:c.3598C>G
|
XP_011520938.1:p.Arg1200Gly
|
|
XM_011522636.2:c.3598C>G
|
XP_011520938.1:p.Arg1200Gly
|
|
XM_011522637.1:c.3595C>G
|
XP_011520939.1:p.Arg1199Gly
|
|
XM_011522637.2:c.3595C>G
|
XP_011520939.1:p.Arg1199Gly
|
|
XM_011522638.1:c.3487C>G
|
XP_011520940.1:p.Arg1163Gly
|
|
XM_011522638.2:c.3760C>G
|
XP_011520940.2:p.Arg1254Gly
|
|
XM_011522639.1:c.3469C>G
|
XP_011520941.1:p.Arg1157Gly
|
|
XM_011522639.2:c.3469C>G
|
XP_011520941.1:p.Arg1157Gly
|
|
XM_011522640.1:c.3466C>G
|
XP_011520942.1:p.Arg1156Gly
|
|
XM_011522640.2:c.3466C>G
|
XP_011520942.1:p.Arg1156Gly
|
|
XM_011522641.1:c.3358C>G
|
XP_011520943.1:p.Arg1120Gly
|
|
XM_017023615.1:c.3595C>G
|
XP_016879104.1:p.Arg1199Gly
|
|
XM_017023616.1:c.3466C>G
|
XP_016879105.1:p.Arg1156Gly
|
|
XM_017023617.1:c.3631C>G
|
XP_016879106.1:p.Arg1211Gly
|
|
XM_017023618.1:c.2254C>G
|
XP_016879107.1:p.Arg752Gly
|
|
XM_024450413.1:c.3466C>G
|
XP_024306181.1:p.Arg1156Gly
|
