|
ENST00000700029.2:c.617_621del
|
ENSP00000514759.2:p.Phe206TrpfsTer?
|
|
|
ENST00000710265.1:c.617_621del
|
ENSP00000518161.1:p.Phe206TrpfsTer?
|
|
|
ENST00000472832.3:c.617_621del
|
ENSP00000483066.2:p.Phe206TrpfsTer?
|
|
|
ENST00000688158.2:n.1352_1356del
|
|
|
|
ENST00000688922.2:c.*447_*451del
|
ENSP00000508742.2:n.*447_*451del
|
|
|
ENST00000700021.1:c.572_576del
|
ENSP00000514757.1:p.Phe191TrpfsTer?
|
|
|
ENST00000700022.1:c.493-5611_493-5607del
|
ENSP00000514758.1:n.493-5611_493-5607del
|
|
|
ENST00000700023.1:n.1775_1779del
|
|
|
|
ENST00000700024.1:n.2009_2013del
|
|
|
|
ENST00000700025.1:n.1386_1390del
|
|
|
|
ENST00000700029.1:c.451_455del
|
|
|
|
ENST00000706954.1:c.617_621del
|
ENSP00000516674.1:p.Phe206TrpfsTer?
|
|
|
ENST00000706955.1:c.*652_*656del
|
ENSP00000516675.1:n.*652_*656del
|
|
|
ENST00000686459.1:c.*203_*207del
|
ENSP00000508909.1:n.*203_*207del
|
|
|
ENST00000688158.1:c.*728_*732del
|
ENSP00000509254.1:n.*728_*732del
|
|
|
ENST00000688308.1:c.617_621del
|
ENSP00000508752.1:p.Phe206TrpfsTer?
|
|
|
ENST00000688922.1:c.538_542del
|
|
|
|
ENST00000693560.1:c.1136_1140del
|
ENSP00000509861.1:p.Phe379TrpfsTer?
|
|
|
ENST00000371953.8:c.617_621del
MANE Select
|
ENSP00000361021.3:p.Phe206TrpfsTer?
|
|
|
ENST00000371953.7:c.617_621del
|
ENSP00000361021.3:p.Phe206TrpfsTer?
|
|
|
ENST00000472832.2:c.44_48del
|
ENSP00000483066.1:p.Phe15TrpfsTer?
|
|
|
NM_000314.5:c.617_621del
|
NP_000305.3:p.Phe206TrpfsTer?
|
|
|
NM_000314.6:c.617_621del
|
NP_000305.3:p.Phe206TrpfsTer?
|
|
|
NM_001304717.2:c.1136_1140del
|
NP_001291646.2:p.Phe379TrpfsTer?
|
|
|
NM_001304718.1:c.26_30del
|
NP_001291647.1:p.Phe9TrpfsTer?
|
|
|
XM_006717926.2:c.572_576del
|
XP_006717989.1:p.Phe191TrpfsTer?
|
|
|
XM_011539981.1:c.617_621del
|
XP_011538283.1:p.Phe206TrpfsTer?
|
|
|
XM_011539982.1:c.521_525del
|
XP_011538284.1:p.Phe174TrpfsTer?
|
|
|
XR_945791.1:n.1205-5611_1205-5607del
|
|
|
|
NM_000314.7:c.617_621del
|
NP_000305.3:p.Phe206TrpfsTer?
|
|
|
NM_001304717.5:c.1136_1140del
|
NP_001291646.4:p.Phe379TrpfsTer?
|
|
|
NM_001304718.2:c.26_30del
|
NP_001291647.1:p.Phe9TrpfsTer?
|
|
|
NM_000314.8:c.617_621del
MANE Select
|
NP_000305.3:p.Phe206TrpfsTer?
|
|
