ENST00000525346.6:c.1008C>A
|
ENSP00000435707.3:p.His336Gln
|
|
ENST00000526780.6:c.1008C>A
|
ENSP00000435668.2:p.His336Gln
|
|
ENST00000527316.6:c.834C>A
|
ENSP00000435047.2:p.His278Gln
|
|
ENST00000682708.1:c.1059C>A
|
ENSP00000506866.1:p.His353Gln
|
|
ENST00000683287.1:c.1044C>A
|
ENSP00000507607.1:p.His348Gln
|
|
ENST00000683714.1:c.1016C>A
|
ENSP00000508207.1:p.Thr339Lys
|
|
ENST00000684396.1:n.1048C>A
|
|
|
ENST00000685320.1:c.423C>A
|
ENSP00000509319.1:p.His141Gln
|
|
ENST00000690257.1:c.912C>A
|
ENSP00000510750.1:p.His304Gln
|
|
ENST00000355527.8:c.1008C>A
MANE Select
|
ENSP00000347717.4:p.His336Gln
|
|
ENST00000355527.7:c.1008C>A
|
ENSP00000347717.3:p.His336Gln
|
|
ENST00000407721.6:c.1008C>A
|
ENSP00000384739.2:p.His336Gln
|
|
ENST00000525137.1:c.509C>A
|
ENSP00000435956.1:p.Thr170Lys
|
|
ENST00000533800.5:c.258C>A
|
ENSP00000435011.1:p.His86Gln
|
|
ENST00000534795.5:c.319+2017C>A
|
|
|
NM_001163817.1:c.1008C>A
|
NP_001157289.1:p.His336Gln
|
|
NM_001360.2:c.1008C>A , LRG_340t1:c.1008C>A
|
NP_001351.2:p.His336Gln
|
|
XM_011544777.1:c.1142C>A
|
XP_011543079.1:p.Thr381Lys
|
|
XM_011544777.2:c.1142C>A
|
XP_011543079.1:p.Thr381Lys
|
|
NM_001163817.2:c.1008C>A
|
NP_001157289.1:p.His336Gln
|
|
NM_001360.3:c.1008C>A
MANE Select
|
NP_001351.2:p.His336Gln
|
|