ENST00000525346.6:c.896A>G
|
ENSP00000435707.3:p.His299Arg
|
|
ENST00000526780.6:c.896A>G
|
ENSP00000435668.2:p.His299Arg
|
|
ENST00000527316.6:c.722A>G
|
ENSP00000435047.2:p.His241Arg
|
|
ENST00000682708.1:c.947A>G
|
ENSP00000506866.1:p.His316Arg
|
|
ENST00000682880.1:c.896A>G
|
ENSP00000507520.1:p.His299Arg
|
|
ENST00000683287.1:c.932A>G
|
ENSP00000507607.1:p.His311Arg
|
|
ENST00000683714.1:c.896A>G
|
ENSP00000508207.1:p.His299Arg
|
|
ENST00000684396.1:n.936A>G
|
|
|
ENST00000685320.1:c.311A>G
|
ENSP00000509319.1:p.His104Arg
|
|
ENST00000690257.1:c.800A>G
|
ENSP00000510750.1:p.His267Arg
|
|
ENST00000355527.8:c.896A>G
MANE Select
|
ENSP00000347717.4:p.His299Arg
|
|
ENST00000355527.7:c.896A>G
|
ENSP00000347717.3:p.His299Arg
|
|
ENST00000407721.6:c.896A>G
|
ENSP00000384739.2:p.His299Arg
|
|
ENST00000525137.1:c.263A>G
|
ENSP00000435956.1:p.His88Arg
|
|
ENST00000533800.5:c.146A>G
|
ENSP00000435011.1:p.His49Arg
|
|
ENST00000534795.5:c.252A>G
|
|
|
NM_001163817.1:c.896A>G
|
NP_001157289.1:p.His299Arg
|
|
NM_001360.2:c.896A>G , LRG_340t1:c.896A>G
|
NP_001351.2:p.His299Arg
|
|
XM_011544777.1:c.896A>G
|
XP_011543079.1:p.His299Arg
|
|
XM_011544777.2:c.896A>G
|
XP_011543079.1:p.His299Arg
|
|
NM_001163817.2:c.896A>G
|
NP_001157289.1:p.His299Arg
|
|
NM_001360.3:c.896A>G
MANE Select
|
NP_001351.2:p.His299Arg
|
|