ENST00000682766.1:c.1364-1438C>A
(TRIM25)
|
ENSP00000507876.1:n.1364-1438C>A
|
|
ENST00000284061.8:c.1135G>T
(DGKE)
MANE Select
|
ENSP00000284061.3:p.Asp379Tyr
|
|
ENST00000648772.1:c.1364-1438C>A
(TRIM25)
|
ENSP00000498158.1:n.1364-1438C>A
|
|
ENST00000284061.7:c.1135G>T
(DGKE)
|
ENSP00000284061.3:p.Asp379Tyr
|
|
ENST00000572944.1:c.965G>T
(DGKE)
|
|
|
NM_003647.2:c.1135G>T
(DGKE)
|
NP_003638.1:p.Asp379Tyr
|
|
XM_011525394.1:c.1189G>T
(DGKE)
|
XP_011523696.1:p.Asp397Tyr
|
|
XM_011525395.1:c.1189G>T
(DGKE)
|
XP_011523697.1:p.Asp397Tyr
|
|
XM_011525396.1:c.1189G>T
(DGKE)
|
XP_011523698.1:p.Asp397Tyr
|
|
XM_011525397.1:c.1189G>T
(DGKE)
|
XP_011523699.1:p.Asp397Tyr
|
|
XM_011525398.1:c.679G>T
(DGKE)
|
XP_011523700.1:p.Asp227Tyr
|
|
XR_934581.1:n.1288G>T
(DGKE)
|
|
|
XM_011525394.3:c.1189G>T
(DGKE)
|
XP_011523696.1:p.Asp397Tyr
|
|
XM_011525395.2:c.1189G>T
(DGKE)
|
XP_011523697.1:p.Asp397Tyr
|
|
XM_011525396.2:c.1189G>T
(DGKE)
|
XP_011523698.1:p.Asp397Tyr
|
|
XM_017025243.2:c.1507G>T
(DGKE)
|
XP_016880732.1:p.Asp503Tyr
|
|
XM_017025244.2:c.1189G>T
(DGKE)
|
XP_016880733.1:p.Asp397Tyr
|
|
XR_001752670.2:n.1693G>T
(DGKE)
|
|
|
XR_001752671.1:n.1300G>T
(DGKE)
|
|
|
XR_001752672.1:n.1301G>T
(DGKE)
|
|
|
XR_002958079.1:n.1299G>T
(DGKE)
|
|
|
NM_003647.3:c.1135G>T
(DGKE)
MANE Select
|
NP_003638.1:p.Asp379Tyr
|
|