ENST00000682775.1:c.2185+12930_2185+12933delinsAGAG
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ENSP00000508399.1:n.2185+12930_2185+12933...
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ENST00000682944.1:c.3048_3051delinsAGAG
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ENSP00000507173.1:p.Glu1016=
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ENST00000683210.1:c.2185+12930_2185+12933delinsAGAG
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ENSP00000506739.1:n.2185+12930_2185+12933...
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ENST00000683270.1:c.3012_3015delinsAGAG
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ENSP00000507624.1:p.Glu1004=
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ENST00000683367.1:c.2177-11371_2177-11368delinsAGAG
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ENSP00000507780.1:n.2177-11371_2177-11368...
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ENST00000683489.1:c.2291+730_2291+733delinsAGAG
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ENSP00000508403.1:n.2291+730_2291+733deli...
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ENST00000683680.1:c.2318+730_2318+733delinsAGAG
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ENSP00000507223.1:n.2318+730_2318+733deli...
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ENST00000684163.1:c.2203+5956_2203+5959delinsAGAG
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ENSP00000508262.1:n.2203+5956_2203+5959de...
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ENST00000684196.1:n.4543-11371_4543-11368delinsAGAG
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ENST00000684325.1:c.2185+12930_2185+12933delinsAGAG
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ENSP00000508121.1:n.2185+12930_2185+12933...
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ENST00000684385.1:c.2220+5956_2220+5959delinsAGAG
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ENSP00000507855.1:n.2220+5956_2220+5959de...
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ENST00000684497.1:c.2185+12930_2185+12933delinsAGAG
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ENSP00000507057.1:n.2185+12930_2185+12933...
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ENST00000382292.9:c.3021_3024delinsAGAG
MANE Select
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ENSP00000371729.3:p.Glu1007=
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ENST00000423156.2:c.2186-11371_2186-11368delinsAGAG
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ENSP00000390925.2:n.2186-11371_2186-11368...
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ENST00000455470.6:c.2431+590_2431+593delinsAGAG
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ENSP00000406565.2:n.2431+590_2431+593deli...
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ENST00000382292.7:c.3021_3024delinsAGAG
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ENSP00000371729.3:p.Glu1007=
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ENST00000382298.7:c.3021_3024delinsAGAG
|
ENSP00000371735.3:p.Glu1007=
|
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ENST00000402364.1:c.771_774delinsAGAG
|
ENSP00000385844.1:p.Glu257=
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ENST00000423156.1:c.1058-11371_1058-11368delinsAGAG
|
ENSP00000390925.1:n.1058-11371_1058-11368...
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ENST00000455470.5:c.2129+590_2129+593delinsAGAG
|
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NM_001278055.1:c.2580_2583delinsAGAG
|
NP_001264984.1:p.Glu860=
|
|
NM_014363.5:c.3021_3024delinsAGAG
|
NP_055178.3:p.Glu1007=
|
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XM_005266338.1:c.3048_3051delinsAGAG
|
XP_005266395.1:p.Glu1016=
|
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XM_011535038.1:c.3072_3075delinsAGAG
|
XP_011533340.1:p.Glu1024=
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XM_011535039.1:c.3039_3042delinsAGAG
|
XP_011533341.1:p.Glu1013=
|
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XM_005266338.2:c.3048_3051delinsAGAG
|
XP_005266395.1:p.Glu1016=
|
|
XM_011535039.2:c.3039_3042delinsAGAG
|
XP_011533341.1:p.Glu1013=
|
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XM_017020539.1:c.3012_3015delinsAGAG
|
XP_016876028.1:p.Glu1004=
|
|
XM_024449337.1:c.3048_3051delinsAGAG
|
XP_024305105.1:p.Glu1016=
|
|
NM_014363.6:c.3021_3024delinsAGAG
MANE Select
|
NP_055178.3:p.Glu1007=
|
|
NM_001278055.2:c.2580_2583delinsAGAG
|
NP_001264984.1:p.Glu860=
|
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