ENST00000525346.6:c.1007A>G
|
ENSP00000435707.3:p.His336Arg
|
|
ENST00000526780.6:c.1007A>G
|
ENSP00000435668.2:p.His336Arg
|
|
ENST00000527316.6:c.833A>G
|
ENSP00000435047.2:p.His278Arg
|
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ENST00000682708.1:c.1058A>G
|
ENSP00000506866.1:p.His353Arg
|
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ENST00000683287.1:c.1043A>G
|
ENSP00000507607.1:p.His348Arg
|
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ENST00000683714.1:c.1015A>G
|
ENSP00000508207.1:p.Thr339Ala
|
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ENST00000684396.1:n.1047A>G
|
|
|
ENST00000685320.1:c.422A>G
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ENSP00000509319.1:p.His141Arg
|
|
ENST00000690257.1:c.911A>G
|
ENSP00000510750.1:p.His304Arg
|
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ENST00000355527.8:c.1007A>G
MANE Select
|
ENSP00000347717.4:p.His336Arg
|
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ENST00000355527.7:c.1007A>G
|
ENSP00000347717.3:p.His336Arg
|
|
ENST00000407721.6:c.1007A>G
|
ENSP00000384739.2:p.His336Arg
|
|
ENST00000525137.1:c.508A>G
|
ENSP00000435956.1:p.Thr170Ala
|
|
ENST00000533800.5:c.257A>G
|
ENSP00000435011.1:p.His86Arg
|
|
ENST00000534795.5:c.319+2016A>G
|
|
|
NM_001163817.1:c.1007A>G
|
NP_001157289.1:p.His336Arg
|
|
NM_001360.2:c.1007A>G , LRG_340t1:c.1007A>G
|
NP_001351.2:p.His336Arg
|
|
XM_011544777.1:c.1141A>G
|
XP_011543079.1:p.Thr381Ala
|
|
XM_011544777.2:c.1141A>G
|
XP_011543079.1:p.Thr381Ala
|
|
NM_001163817.2:c.1007A>G
|
NP_001157289.1:p.His336Arg
|
|
NM_001360.3:c.1007A>G
MANE Select
|
NP_001351.2:p.His336Arg
|
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