ENST00000525346.6:c.1119G=
|
ENSP00000435707.3:p.Arg373=
|
|
ENST00000526780.6:c.1119G=
|
ENSP00000435668.2:p.Arg373=
|
|
ENST00000527316.6:c.945G=
|
ENSP00000435047.2:p.Arg315=
|
|
ENST00000682708.1:c.1170G=
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ENSP00000506866.1:p.Arg390=
|
|
ENST00000683287.1:c.1155G=
|
ENSP00000507607.1:p.Arg385=
|
|
ENST00000683714.1:c.1127G=
|
ENSP00000508207.1:p.Gly376=
|
|
ENST00000684396.1:n.1159G=
|
|
|
ENST00000685320.1:c.534G=
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ENSP00000509319.1:p.Arg178=
|
|
ENST00000690257.1:c.1023G=
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ENSP00000510750.1:p.Arg341=
|
|
ENST00000355527.8:c.1119G=
MANE Select
|
ENSP00000347717.4:p.Arg373=
|
|
ENST00000355527.7:c.1119G=
|
ENSP00000347717.3:p.Arg373=
|
|
ENST00000407721.6:c.1119G=
|
ENSP00000384739.2:p.Arg373=
|
|
ENST00000525137.1:c.620G=
|
ENSP00000435956.1:p.Gly207=
|
|
ENST00000533800.5:c.369G=
|
ENSP00000435011.1:p.Arg123=
|
|
ENST00000534795.5:c.319+2128G=
|
|
|
NM_001163817.1:c.1119G=
|
NP_001157289.1:p.Arg373=
|
|
NM_001360.2:c.1119G= , LRG_340t1:c.1119G=
|
NP_001351.2:p.Arg373=
|
|
XM_011544777.1:c.1253G=
|
XP_011543079.1:p.Gly418=
|
|
XM_011544777.2:c.1253G=
|
XP_011543079.1:p.Gly418=
|
|
NM_001163817.2:c.1119G=
|
NP_001157289.1:p.Arg373=
|
|
NM_001360.3:c.1119G=
MANE Select
|
NP_001351.2:p.Arg373=
|
|