|
ENST00000700029.2:c.970G>T
|
ENSP00000514759.2:p.Gly324Ter
|
|
|
ENST00000710265.1:c.877G>T
|
ENSP00000518161.1:p.Gly293Ter
|
|
|
ENST00000472832.3:c.877G>T
|
ENSP00000483066.2:p.Gly293Ter
|
|
|
ENST00000688158.2:n.1612G>T
|
|
|
|
ENST00000688922.2:c.*707G>T
|
ENSP00000508742.2:n.*707G>T
|
|
|
ENST00000700021.1:c.832G>T
|
ENSP00000514757.1:p.Gly278Ter
|
|
|
ENST00000700022.1:c.*216G>T
|
ENSP00000514758.1:n.*216G>T
|
|
|
ENST00000700023.1:n.2035G>T
|
|
|
|
ENST00000700024.1:n.2269G>T
|
|
|
|
ENST00000700025.1:n.1646G>T
|
|
|
|
ENST00000700026.1:n.514G>T
|
|
|
|
ENST00000700029.1:c.804G>T
|
|
|
|
ENST00000706954.1:c.877G>T
|
ENSP00000516674.1:p.Gly293Ter
|
|
|
ENST00000706955.1:c.*912G>T
|
ENSP00000516675.1:n.*912G>T
|
|
|
ENST00000686459.1:c.*463G>T
|
ENSP00000508909.1:n.*463G>T
|
|
|
ENST00000688158.1:c.*988G>T
|
ENSP00000509254.1:n.*988G>T
|
|
|
ENST00000688308.1:c.877G>T
|
ENSP00000508752.1:p.Gly293Ter
|
|
|
ENST00000688922.1:c.798G>T
|
|
|
|
ENST00000693560.1:c.1396G>T
|
ENSP00000509861.1:p.Gly466Ter
|
|
|
ENST00000371953.8:c.877G>T
MANE Select
|
ENSP00000361021.3:p.Gly293Ter
|
|
|
ENST00000371953.7:c.877G>T
|
ENSP00000361021.3:p.Gly293Ter
|
|
|
ENST00000472832.2:c.304G>T
|
ENSP00000483066.1:p.Gly102Ter
|
|
|
NM_000314.5:c.877G>T
|
NP_000305.3:p.Gly293Ter
|
|
|
NM_000314.6:c.877G>T
|
NP_000305.3:p.Gly293Ter
|
|
|
NM_001304717.2:c.1396G>T
|
NP_001291646.2:p.Gly466Ter
|
|
|
NM_001304718.1:c.286G>T
|
NP_001291647.1:p.Gly96Ter
|
|
|
XM_006717926.2:c.832G>T
|
XP_006717989.1:p.Gly278Ter
|
|
|
XM_011539981.1:c.877G>T
|
XP_011538283.1:p.Gly293Ter
|
|
|
XM_011539982.1:c.781G>T
|
XP_011538284.1:p.Gly261Ter
|
|
|
XR_945791.1:n.1447G>T
|
|
|
|
NM_000314.7:c.877G>T
|
NP_000305.3:p.Gly293Ter
|
|
|
NM_001304717.5:c.1396G>T
|
NP_001291646.4:p.Gly466Ter
|
|
|
NM_001304718.2:c.286G>T
|
NP_001291647.1:p.Gly96Ter
|
|
|
NM_000314.8:c.877G>T
MANE Select
|
NP_000305.3:p.Gly293Ter
|
|
