ENST00000525346.6:c.982C>T
|
ENSP00000435707.3:p.His328Tyr
|
|
ENST00000526780.6:c.982C>T
|
ENSP00000435668.2:p.His328Tyr
|
|
ENST00000527316.6:c.808C>T
|
ENSP00000435047.2:p.His270Tyr
|
|
ENST00000682708.1:c.1033C>T
|
ENSP00000506866.1:p.His345Tyr
|
|
ENST00000683287.1:c.1018C>T
|
ENSP00000507607.1:p.His340Tyr
|
|
ENST00000683714.1:c.990C>T
|
ENSP00000508207.1:p.Thr330=
|
|
ENST00000684396.1:n.1022C>T
|
|
|
ENST00000685320.1:c.397C>T
|
ENSP00000509319.1:p.His133Tyr
|
|
ENST00000690257.1:c.886C>T
|
ENSP00000510750.1:p.His296Tyr
|
|
ENST00000355527.8:c.982C>T
MANE Select
|
ENSP00000347717.4:p.His328Tyr
|
|
ENST00000355527.7:c.982C>T
|
ENSP00000347717.3:p.His328Tyr
|
|
ENST00000407721.6:c.982C>T
|
ENSP00000384739.2:p.His328Tyr
|
|
ENST00000525137.1:c.483C>T
|
ENSP00000435956.1:p.Thr161=
|
|
ENST00000533800.5:c.232C>T
|
ENSP00000435011.1:p.His78Tyr
|
|
ENST00000534795.5:c.319+1991C>T
|
|
|
NM_001163817.1:c.982C>T
|
NP_001157289.1:p.His328Tyr
|
|
NM_001360.2:c.982C>T , LRG_340t1:c.982C>T
|
NP_001351.2:p.His328Tyr
|
|
XM_011544777.1:c.1116C>T
|
XP_011543079.1:p.Thr372=
|
|
XM_011544777.2:c.1116C>T
|
XP_011543079.1:p.Thr372=
|
|
NM_001163817.2:c.982C>T
|
NP_001157289.1:p.His328Tyr
|
|
NM_001360.3:c.982C>T
MANE Select
|
NP_001351.2:p.His328Tyr
|
|