|
ENST00000700029.2:c.782_783delinsAG
|
ENSP00000514759.2:p.Gln261=
|
|
|
ENST00000710265.1:c.782_783delinsAG
|
ENSP00000518161.1:p.Gln261=
|
|
|
ENST00000472832.3:c.782_783delinsAG
|
ENSP00000483066.2:p.Gln261=
|
|
|
ENST00000688158.2:n.1517_1518delinsAG
|
|
|
|
ENST00000688922.2:c.*612_*613delinsAG
|
ENSP00000508742.2:n.*612_*613delinsAG
|
|
|
ENST00000700021.1:c.737_738delinsAG
|
ENSP00000514757.1:p.Gln246=
|
|
|
ENST00000700022.1:c.*121_*122delinsAG
|
ENSP00000514758.1:n.*121_*122delinsAG
|
|
|
ENST00000700023.1:n.1940_1941delinsAG
|
|
|
|
ENST00000700024.1:n.2174_2175delinsAG
|
|
|
|
ENST00000700025.1:n.1551_1552delinsAG
|
|
|
|
ENST00000700026.1:n.419_420delinsAG
|
|
|
|
ENST00000700029.1:c.616_617delinsAG
|
|
|
|
ENST00000706954.1:c.782_783delinsAG
|
ENSP00000516674.1:p.Gln261=
|
|
|
ENST00000706955.1:c.*817_*818delinsAG
|
ENSP00000516675.1:n.*817_*818delinsAG
|
|
|
ENST00000686459.1:c.*368_*369delinsAG
|
ENSP00000508909.1:n.*368_*369delinsAG
|
|
|
ENST00000688158.1:c.*893_*894delinsAG
|
ENSP00000509254.1:n.*893_*894delinsAG
|
|
|
ENST00000688308.1:c.782_783delinsAG
|
ENSP00000508752.1:p.Gln261=
|
|
|
ENST00000688922.1:c.703_704delinsAG
|
|
|
|
ENST00000693560.1:c.1301_1302delinsAG
|
ENSP00000509861.1:p.Gln434=
|
|
|
ENST00000371953.8:c.782_783delinsAG
MANE Select
|
ENSP00000361021.3:p.Gln261=
|
|
|
ENST00000371953.7:c.782_783delinsAG
|
ENSP00000361021.3:p.Gln261=
|
|
|
ENST00000472832.2:c.209_210delinsAG
|
ENSP00000483066.1:p.Gln70=
|
|
|
NM_000314.5:c.782_783delinsAG
|
NP_000305.3:p.Gln261=
|
|
|
NM_000314.6:c.782_783delinsAG
|
NP_000305.3:p.Gln261=
|
|
|
NM_001304717.2:c.1301_1302delinsAG
|
NP_001291646.2:p.Gln434=
|
|
|
NM_001304718.1:c.191_192delinsAG
|
NP_001291647.1:p.Gln64=
|
|
|
XM_006717926.2:c.737_738delinsAG
|
XP_006717989.1:p.Gln246=
|
|
|
XM_011539981.1:c.782_783delinsAG
|
XP_011538283.1:p.Gln261=
|
|
|
XM_011539982.1:c.686_687delinsAG
|
XP_011538284.1:p.Gln229=
|
|
|
XR_945791.1:n.1352_1353delinsAG
|
|
|
|
NM_000314.7:c.782_783delinsAG
|
NP_000305.3:p.Gln261=
|
|
|
NM_001304717.5:c.1301_1302delinsAG
|
NP_001291646.4:p.Gln434=
|
|
|
NM_001304718.2:c.191_192delinsAG
|
NP_001291647.1:p.Gln64=
|
|
|
NM_000314.8:c.782_783delinsAG
MANE Select
|
NP_000305.3:p.Gln261=
|
|
