ENST00000682766.1:c.1364-1446G>A
(TRIM25)
|
ENSP00000507876.1:n.1364-1446G>A
|
|
ENST00000284061.8:c.1143C>T
(DGKE)
MANE Select
|
ENSP00000284061.3:p.Leu381=
|
|
ENST00000648772.1:c.1364-1446G>A
(TRIM25)
|
ENSP00000498158.1:n.1364-1446G>A
|
|
ENST00000284061.7:c.1143C>T
(DGKE)
|
ENSP00000284061.3:p.Leu381=
|
|
ENST00000572944.1:c.973C>T
(DGKE)
|
|
|
NM_003647.2:c.1143C>T
(DGKE)
|
NP_003638.1:p.Leu381=
|
|
XM_011525394.1:c.1197C>T
(DGKE)
|
XP_011523696.1:p.Leu399=
|
|
XM_011525395.1:c.1197C>T
(DGKE)
|
XP_011523697.1:p.Leu399=
|
|
XM_011525396.1:c.1197C>T
(DGKE)
|
XP_011523698.1:p.Leu399=
|
|
XM_011525397.1:c.1197C>T
(DGKE)
|
XP_011523699.1:p.Leu399=
|
|
XM_011525398.1:c.687C>T
(DGKE)
|
XP_011523700.1:p.Leu229=
|
|
XR_934581.1:n.1296C>T
(DGKE)
|
|
|
XM_011525394.3:c.1197C>T
(DGKE)
|
XP_011523696.1:p.Leu399=
|
|
XM_011525395.2:c.1197C>T
(DGKE)
|
XP_011523697.1:p.Leu399=
|
|
XM_011525396.2:c.1197C>T
(DGKE)
|
XP_011523698.1:p.Leu399=
|
|
XM_017025243.2:c.1515C>T
(DGKE)
|
XP_016880732.1:p.Leu505=
|
|
XM_017025244.2:c.1197C>T
(DGKE)
|
XP_016880733.1:p.Leu399=
|
|
XR_001752670.2:n.1701C>T
(DGKE)
|
|
|
XR_001752671.1:n.1308C>T
(DGKE)
|
|
|
XR_001752672.1:n.1309C>T
(DGKE)
|
|
|
XR_002958079.1:n.1307C>T
(DGKE)
|
|
|
NM_003647.3:c.1143C>T
(DGKE)
MANE Select
|
NP_003638.1:p.Leu381=
|
|