ENST00000525346.6:c.1145A=
|
ENSP00000435707.3:p.Tyr382=
|
|
ENST00000526780.6:c.1145A=
|
ENSP00000435668.2:p.Tyr382=
|
|
ENST00000527316.6:c.971A=
|
ENSP00000435047.2:p.Tyr324=
|
|
ENST00000682708.1:c.1196A=
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ENSP00000506866.1:p.Tyr399=
|
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ENST00000683287.1:c.1181A=
|
ENSP00000507607.1:p.Tyr394=
|
|
ENST00000683714.1:c.1153A=
|
ENSP00000508207.1:p.Thr385=
|
|
ENST00000684396.1:n.1185A=
|
|
|
ENST00000685320.1:c.560A=
|
ENSP00000509319.1:p.Tyr187=
|
|
ENST00000690257.1:c.1049A=
|
ENSP00000510750.1:p.Tyr350=
|
|
ENST00000355527.8:c.1145A=
MANE Select
|
ENSP00000347717.4:p.Tyr382=
|
|
ENST00000355527.7:c.1145A=
|
ENSP00000347717.3:p.Tyr382=
|
|
ENST00000407721.6:c.1145A=
|
ENSP00000384739.2:p.Tyr382=
|
|
ENST00000525137.1:c.646A=
|
ENSP00000435956.1:p.Thr216=
|
|
ENST00000533800.5:c.395A=
|
ENSP00000435011.1:p.Tyr132=
|
|
ENST00000534795.5:c.319+2154A=
|
|
|
NM_001163817.1:c.1145A=
|
NP_001157289.1:p.Tyr382=
|
|
NM_001360.2:c.1145A= , LRG_340t1:c.1145A=
|
NP_001351.2:p.Tyr382=
|
|
XM_011544777.1:c.1279A=
|
XP_011543079.1:p.Thr427=
|
|
XM_011544777.2:c.1279A=
|
XP_011543079.1:p.Thr427=
|
|
NM_001163817.2:c.1145A=
|
NP_001157289.1:p.Tyr382=
|
|
NM_001360.3:c.1145A=
MANE Select
|
NP_001351.2:p.Tyr382=
|
|