ENST00000525346.6:c.963+86G>T
|
ENSP00000435707.3:n.963+86G>T
|
|
ENST00000526780.6:c.963+86G>T
|
ENSP00000435668.2:n.963+86G>T
|
|
ENST00000527316.6:c.789+86G>T
|
ENSP00000435047.2:n.789+86G>T
|
|
ENST00000682708.1:c.1014+86G>T
|
ENSP00000506866.1:n.1014+86G>T
|
|
ENST00000682880.1:c.1049G>T
|
ENSP00000507520.1:p.Gly350Val
|
|
ENST00000683287.1:c.999+86G>T
|
ENSP00000507607.1:n.999+86G>T
|
|
ENST00000683714.1:c.971+78G>T
|
ENSP00000508207.1:n.971+78G>T
|
|
ENST00000684396.1:n.1003+86G>T
|
|
|
ENST00000685320.1:c.378+86G>T
|
ENSP00000509319.1:n.378+86G>T
|
|
ENST00000690257.1:c.867+86G>T
|
ENSP00000510750.1:n.867+86G>T
|
|
ENST00000355527.8:c.963+86G>T
MANE Select
|
ENSP00000347717.4:n.963+86G>T
|
|
ENST00000355527.7:c.963+86G>T
|
ENSP00000347717.3:n.963+86G>T
|
|
ENST00000407721.6:c.963+86G>T
|
ENSP00000384739.2:n.963+86G>T
|
|
ENST00000525137.1:c.330+86G>T
|
ENSP00000435956.1:n.330+86G>T
|
|
ENST00000533800.5:c.213+86G>T
|
ENSP00000435011.1:n.213+86G>T
|
|
ENST00000534795.5:c.319+86G>T
|
|
|
NM_001163817.1:c.963+86G>T
|
NP_001157289.1:n.963+86G>T
|
|
NM_001360.2:c.963+86G>T , LRG_340t1:c.963+86G>T
|
NP_001351.2:n.963+86G>T
|
|
XM_011544777.1:c.963+86G>T
|
XP_011543079.1:n.963+86G>T
|
|
XM_011544777.2:c.963+86G>T
|
XP_011543079.1:n.963+86G>T
|
|
NM_001163817.2:c.963+86G>T
|
NP_001157289.1:n.963+86G>T
|
|
NM_001360.3:c.963+86G>T
MANE Select
|
NP_001351.2:n.963+86G>T
|
|