ENST00000525346.6:c.971A=
|
ENSP00000435707.3:p.Tyr324=
|
|
ENST00000526780.6:c.971A=
|
ENSP00000435668.2:p.Tyr324=
|
|
ENST00000527316.6:c.797A=
|
ENSP00000435047.2:p.Tyr266=
|
|
ENST00000682708.1:c.1022A=
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ENSP00000506866.1:p.Tyr341=
|
|
ENST00000683287.1:c.1007A=
|
ENSP00000507607.1:p.Tyr336=
|
|
ENST00000683714.1:c.979A=
|
ENSP00000508207.1:p.Thr327=
|
|
ENST00000684396.1:n.1011A=
|
|
|
ENST00000685320.1:c.386A=
|
ENSP00000509319.1:p.Tyr129=
|
|
ENST00000690257.1:c.875A=
|
ENSP00000510750.1:p.Tyr292=
|
|
ENST00000355527.8:c.971A=
MANE Select
|
ENSP00000347717.4:p.Tyr324=
|
|
ENST00000355527.7:c.971A=
|
ENSP00000347717.3:p.Tyr324=
|
|
ENST00000407721.6:c.971A=
|
ENSP00000384739.2:p.Tyr324=
|
|
ENST00000525137.1:c.472A=
|
ENSP00000435956.1:p.Thr158=
|
|
ENST00000533800.5:c.221A=
|
ENSP00000435011.1:p.Tyr74=
|
|
ENST00000534795.5:c.319+1980A=
|
|
|
NM_001163817.1:c.971A=
|
NP_001157289.1:p.Tyr324=
|
|
NM_001360.2:c.971A= , LRG_340t1:c.971A=
|
NP_001351.2:p.Tyr324=
|
|
XM_011544777.1:c.1105A=
|
XP_011543079.1:p.Thr369=
|
|
XM_011544777.2:c.1105A=
|
XP_011543079.1:p.Thr369=
|
|
NM_001163817.2:c.971A=
|
NP_001157289.1:p.Tyr324=
|
|
NM_001360.3:c.971A=
MANE Select
|
NP_001351.2:p.Tyr324=
|
|