ENST00000682775.1:c.2185+20406_2185+20409del
|
ENSP00000508399.1:n.2185+20406_2185+20409del
|
|
ENST00000682944.1:c.10524_10527del
|
ENSP00000507173.1:p.Tyr3508Ter
|
|
ENST00000683210.1:c.2185+20406_2185+20409del
|
ENSP00000506739.1:n.2185+20406_2185+20409del
|
|
ENST00000683270.1:c.6446-3895_6446-3892del
|
ENSP00000507624.1:n.6446-3895_6446-3892del
|
|
ENST00000683367.1:c.2177-3895_2177-3892del
|
ENSP00000507780.1:n.2177-3895_2177-3892del
|
|
ENST00000683489.1:c.2292-3427_2292-3424del
|
ENSP00000508403.1:n.2292-3427_2292-3424del
|
|
ENST00000683680.1:c.2319-3427_2319-3424del
|
ENSP00000507223.1:n.2319-3427_2319-3424del
|
|
ENST00000684163.1:c.2204-3895_2204-3892del
|
ENSP00000508262.1:n.2204-3895_2204-3892del
|
|
ENST00000684196.1:n.4543-3895_4543-3892del
|
|
|
ENST00000684325.1:c.2186-11705_2186-11702del
|
ENSP00000508121.1:n.2186-11705_2186-11702del
|
|
ENST00000684385.1:c.2221-3895_2221-3892del
|
ENSP00000507855.1:n.2221-3895_2221-3892del
|
|
ENST00000684497.1:c.2186-10735_2186-10732del
|
ENSP00000507057.1:n.2186-10735_2186-10732del
|
|
ENST00000382292.9:c.10497_10500del
MANE Select
|
ENSP00000371729.3:p.Tyr3499Ter
|
|
ENST00000423156.2:c.2186-3895_2186-3892del
|
ENSP00000390925.2:n.2186-3895_2186-3892del
|
|
ENST00000455470.6:c.2432-3895_2432-3892del
|
ENSP00000406565.2:n.2432-3895_2432-3892del
|
|
ENST00000382292.7:c.10497_10500del
|
ENSP00000371729.3:p.Tyr3499Ter
|
|
ENST00000382298.7:c.10497_10500del
|
ENSP00000371735.3:p.Tyr3499Ter
|
|
ENST00000402364.1:c.8247_8250del
|
ENSP00000385844.1:p.Tyr2749Ter
|
|
ENST00000423156.1:c.1058-3895_1058-3892del
|
ENSP00000390925.1:n.1058-3895_1058-3892del
|
|
ENST00000455470.5:c.2130-3895_2130-3892del
|
|
|
NM_001278055.1:c.10056_10059del
|
NP_001264984.1:p.Tyr3352Ter
|
|
NM_014363.5:c.10497_10500del
|
NP_055178.3:p.Tyr3499Ter
|
|
XM_005266338.1:c.10524_10527del
|
XP_005266395.1:p.Tyr3508Ter
|
|
XM_011535038.1:c.10548_10551del
|
XP_011533340.1:p.Tyr3516Ter
|
|
XM_011535039.1:c.10515_10518del
|
XP_011533341.1:p.Tyr3505Ter
|
|
XM_005266338.2:c.10524_10527del
|
XP_005266395.1:p.Tyr3508Ter
|
|
XM_011535039.2:c.10515_10518del
|
XP_011533341.1:p.Tyr3505Ter
|
|
XM_017020539.1:c.10488_10491del
|
XP_016876028.1:p.Tyr3496Ter
|
|
XM_024449337.1:c.10524_10527del
|
XP_024305105.1:p.Tyr3508Ter
|
|
NM_014363.6:c.10497_10500del
MANE Select
|
NP_055178.3:p.Tyr3499Ter
|
|
NM_001278055.2:c.10056_10059del
|
NP_001264984.1:p.Tyr3352Ter
|
|