|
ENST00000682775.1:c.2185+19686_2185+19689delinsAGAT
|
ENSP00000508399.1:n.2185+19686_2185+19689delinsAGAT
|
|
|
ENST00000682944.1:c.9804_9807delinsAGAT
|
ENSP00000507173.1:p.Glu3268=
|
|
|
ENST00000683210.1:c.2185+19686_2185+19689delinsAGAT
|
ENSP00000506739.1:n.2185+19686_2185+19689delinsAGAT
|
|
|
ENST00000683270.1:c.6445+3323_6445+3326delinsAGAT
|
ENSP00000507624.1:n.6445+3323_6445+3326delinsAGAT
|
|
|
ENST00000683367.1:c.2177-4615_2177-4612delinsAGAT
|
ENSP00000507780.1:n.2177-4615_2177-4612delinsAGAT
|
|
|
ENST00000683489.1:c.2292-4147_2292-4144delinsAGAT
|
ENSP00000508403.1:n.2292-4147_2292-4144delinsAGAT
|
|
|
ENST00000683680.1:c.2319-4147_2319-4144delinsAGAT
|
ENSP00000507223.1:n.2319-4147_2319-4144delinsAGAT
|
|
|
ENST00000684163.1:c.2204-4615_2204-4612delinsAGAT
|
ENSP00000508262.1:n.2204-4615_2204-4612delinsAGAT
|
|
|
ENST00000684196.1:n.4543-4615_4543-4612delinsAGAT
|
|
|
|
ENST00000684325.1:c.2186-12425_2186-12422delinsAGAT
|
ENSP00000508121.1:n.2186-12425_2186-12422delinsAGAT
|
|
|
ENST00000684385.1:c.2221-4615_2221-4612delinsAGAT
|
ENSP00000507855.1:n.2221-4615_2221-4612delinsAGAT
|
|
|
ENST00000684497.1:c.2186-11455_2186-11452delinsAGAT
|
ENSP00000507057.1:n.2186-11455_2186-11452delinsAGAT
|
|
|
ENST00000382292.9:c.9777_9780delinsAGAT
MANE Select
|
ENSP00000371729.3:p.Glu3259=
|
|
|
ENST00000423156.2:c.2186-4615_2186-4612delinsAGAT
|
ENSP00000390925.2:n.2186-4615_2186-4612delinsAGAT
|
|
|
ENST00000455470.6:c.2432-4615_2432-4612delinsAGAT
|
ENSP00000406565.2:n.2432-4615_2432-4612delinsAGAT
|
|
|
ENST00000382292.7:c.9777_9780delinsAGAT
|
ENSP00000371729.3:p.Glu3259=
|
|
|
ENST00000382298.7:c.9777_9780delinsAGAT
|
ENSP00000371735.3:p.Glu3259=
|
|
|
ENST00000402364.1:c.7527_7530delinsAGAT
|
ENSP00000385844.1:p.Glu2509=
|
|
|
ENST00000423156.1:c.1058-4615_1058-4612delinsAGAT
|
ENSP00000390925.1:n.1058-4615_1058-4612delinsAGAT
|
|
|
ENST00000455470.5:c.2130-4615_2130-4612delinsAGAT
|
|
|
|
NM_001278055.1:c.9336_9339delinsAGAT
|
NP_001264984.1:p.Glu3112=
|
|
|
NM_014363.5:c.9777_9780delinsAGAT
|
NP_055178.3:p.Glu3259=
|
|
|
XM_005266338.1:c.9804_9807delinsAGAT
|
XP_005266395.1:p.Glu3268=
|
|
|
XM_011535038.1:c.9828_9831delinsAGAT
|
XP_011533340.1:p.Glu3276=
|
|
|
XM_011535039.1:c.9795_9798delinsAGAT
|
XP_011533341.1:p.Glu3265=
|
|
|
XM_005266338.2:c.9804_9807delinsAGAT
|
XP_005266395.1:p.Glu3268=
|
|
|
XM_011535039.2:c.9795_9798delinsAGAT
|
XP_011533341.1:p.Glu3265=
|
|
|
XM_017020539.1:c.9768_9771delinsAGAT
|
XP_016876028.1:p.Glu3256=
|
|
|
XM_024449337.1:c.9804_9807delinsAGAT
|
XP_024305105.1:p.Glu3268=
|
|
|
NM_014363.6:c.9777_9780delinsAGAT
MANE Select
|
NP_055178.3:p.Glu3259=
|
|
|
NM_001278055.2:c.9336_9339delinsAGAT
|
NP_001264984.1:p.Glu3112=
|
|
