ENST00000525346.6:c.1166G=
|
ENSP00000435707.3:p.Arg389=
|
|
ENST00000526780.6:c.1166G=
|
ENSP00000435668.2:p.Arg389=
|
|
ENST00000527316.6:c.992G=
|
ENSP00000435047.2:p.Arg331=
|
|
ENST00000682708.1:c.1217G=
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ENSP00000506866.1:p.Arg406=
|
|
ENST00000683287.1:c.1202G=
|
ENSP00000507607.1:p.Arg401=
|
|
ENST00000683714.1:c.1174G=
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ENSP00000508207.1:p.Gly392=
|
|
ENST00000684396.1:n.1206G=
|
|
|
ENST00000685320.1:c.581G=
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ENSP00000509319.1:p.Arg194=
|
|
ENST00000690257.1:c.1070G=
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ENSP00000510750.1:p.Arg357=
|
|
ENST00000355527.8:c.1166G=
MANE Select
|
ENSP00000347717.4:p.Arg389=
|
|
ENST00000355527.7:c.1166G=
|
ENSP00000347717.3:p.Arg389=
|
|
ENST00000407721.6:c.1166G=
|
ENSP00000384739.2:p.Arg389=
|
|
ENST00000525137.1:c.667G=
|
ENSP00000435956.1:p.Gly223=
|
|
ENST00000533800.5:c.416G=
|
ENSP00000435011.1:p.Arg139=
|
|
ENST00000534795.5:c.319+2175G=
|
|
|
NM_001163817.1:c.1166G=
|
NP_001157289.1:p.Arg389=
|
|
NM_001360.2:c.1166G= , LRG_340t1:c.1166G=
|
NP_001351.2:p.Arg389=
|
|
XM_011544777.1:c.1300G=
|
XP_011543079.1:p.Gly434=
|
|
XM_011544777.2:c.1300G=
|
XP_011543079.1:p.Gly434=
|
|
NM_001163817.2:c.1166G=
|
NP_001157289.1:p.Arg389=
|
|
NM_001360.3:c.1166G=
MANE Select
|
NP_001351.2:p.Arg389=
|
|