ENST00000525346.6:c.1170C>G
|
ENSP00000435707.3:p.His390Gln
|
|
ENST00000526780.6:c.1170C>G
|
ENSP00000435668.2:p.His390Gln
|
|
ENST00000527316.6:c.996C>G
|
ENSP00000435047.2:p.His332Gln
|
|
ENST00000682708.1:c.1221C>G
|
ENSP00000506866.1:p.His407Gln
|
|
ENST00000683287.1:c.1206C>G
|
ENSP00000507607.1:p.His402Gln
|
|
ENST00000683714.1:c.1178C>G
|
ENSP00000508207.1:p.Thr393Ser
|
|
ENST00000684396.1:n.1210C>G
|
|
|
ENST00000685320.1:c.585C>G
|
ENSP00000509319.1:p.His195Gln
|
|
ENST00000690257.1:c.1074C>G
|
ENSP00000510750.1:p.His358Gln
|
|
ENST00000355527.8:c.1170C>G
MANE Select
|
ENSP00000347717.4:p.His390Gln
|
|
ENST00000355527.7:c.1170C>G
|
ENSP00000347717.3:p.His390Gln
|
|
ENST00000407721.6:c.1170C>G
|
ENSP00000384739.2:p.His390Gln
|
|
ENST00000525137.1:c.671C>G
|
ENSP00000435956.1:p.Thr224Ser
|
|
ENST00000533800.5:c.420C>G
|
ENSP00000435011.1:p.His140Gln
|
|
ENST00000534795.5:c.319+2179C>G
|
|
|
NM_001163817.1:c.1170C>G
|
NP_001157289.1:p.His390Gln
|
|
NM_001360.2:c.1170C>G , LRG_340t1:c.1170C>G
|
NP_001351.2:p.His390Gln
|
|
XM_011544777.1:c.1304C>G
|
XP_011543079.1:p.Thr435Ser
|
|
XM_011544777.2:c.1304C>G
|
XP_011543079.1:p.Thr435Ser
|
|
NM_001163817.2:c.1170C>G
|
NP_001157289.1:p.His390Gln
|
|
NM_001360.3:c.1170C>G
MANE Select
|
NP_001351.2:p.His390Gln
|
|