ENST00000525346.6:c.1168C>A
|
ENSP00000435707.3:p.His390Asn
|
|
ENST00000526780.6:c.1168C>A
|
ENSP00000435668.2:p.His390Asn
|
|
ENST00000527316.6:c.994C>A
|
ENSP00000435047.2:p.His332Asn
|
|
ENST00000682708.1:c.1219C>A
|
ENSP00000506866.1:p.His407Asn
|
|
ENST00000683287.1:c.1204C>A
|
ENSP00000507607.1:p.His402Asn
|
|
ENST00000683714.1:c.1176C>A
|
ENSP00000508207.1:p.Gly392=
|
|
ENST00000684396.1:n.1208C>A
|
|
|
ENST00000685320.1:c.583C>A
|
ENSP00000509319.1:p.His195Asn
|
|
ENST00000690257.1:c.1072C>A
|
ENSP00000510750.1:p.His358Asn
|
|
ENST00000355527.8:c.1168C>A
MANE Select
|
ENSP00000347717.4:p.His390Asn
|
|
ENST00000355527.7:c.1168C>A
|
ENSP00000347717.3:p.His390Asn
|
|
ENST00000407721.6:c.1168C>A
|
ENSP00000384739.2:p.His390Asn
|
|
ENST00000525137.1:c.669C>A
|
ENSP00000435956.1:p.Gly223=
|
|
ENST00000533800.5:c.418C>A
|
ENSP00000435011.1:p.His140Asn
|
|
ENST00000534795.5:c.319+2177C>A
|
|
|
NM_001163817.1:c.1168C>A
|
NP_001157289.1:p.His390Asn
|
|
NM_001360.2:c.1168C>A , LRG_340t1:c.1168C>A
|
NP_001351.2:p.His390Asn
|
|
XM_011544777.1:c.1302C>A
|
XP_011543079.1:p.Gly434=
|
|
XM_011544777.2:c.1302C>A
|
XP_011543079.1:p.Gly434=
|
|
NM_001163817.2:c.1168C>A
|
NP_001157289.1:p.His390Asn
|
|
NM_001360.3:c.1168C>A
MANE Select
|
NP_001351.2:p.His390Asn
|
|