ENST00000284061.8:c.630C>G
(DGKE)
MANE Select
|
ENSP00000284061.3:p.Ala210=
|
|
ENST00000648772.1:c.*314-1905G>C
(TRIM25)
|
ENSP00000498158.1:n.*314-1905G>C
|
|
ENST00000284061.7:c.630C>G
(DGKE)
|
ENSP00000284061.3:p.Ala210=
|
|
ENST00000571084.1:n.166C>G
(DGKE)
|
|
|
ENST00000572944.1:c.460C>G
(DGKE)
|
|
|
ENST00000576869.5:n.778C>G
(DGKE)
|
|
|
NM_003647.2:c.630C>G
(DGKE)
|
NP_003638.1:p.Ala210=
|
|
XM_011525394.1:c.684C>G
(DGKE)
|
XP_011523696.1:p.Ala228=
|
|
XM_011525395.1:c.684C>G
(DGKE)
|
XP_011523697.1:p.Ala228=
|
|
XM_011525396.1:c.684C>G
(DGKE)
|
XP_011523698.1:p.Ala228=
|
|
XM_011525397.1:c.684C>G
(DGKE)
|
XP_011523699.1:p.Ala228=
|
|
XM_011525398.1:c.174C>G
(DGKE)
|
XP_011523700.1:p.Ala58=
|
|
XR_934581.1:n.783C>G
(DGKE)
|
|
|
XM_011525394.3:c.684C>G
(DGKE)
|
XP_011523696.1:p.Ala228=
|
|
XM_011525395.2:c.684C>G
(DGKE)
|
XP_011523697.1:p.Ala228=
|
|
XM_011525396.2:c.684C>G
(DGKE)
|
XP_011523698.1:p.Ala228=
|
|
XM_017025243.2:c.630C>G
(DGKE)
|
XP_016880732.1:p.Ala210=
|
|
XM_017025244.2:c.684C>G
(DGKE)
|
XP_016880733.1:p.Ala228=
|
|
XR_001752670.2:n.816C>G
(DGKE)
|
|
|
XR_001752671.1:n.795C>G
(DGKE)
|
|
|
XR_001752672.1:n.796C>G
(DGKE)
|
|
|
XR_002958079.1:n.794C>G
(DGKE)
|
|
|
NM_003647.3:c.630C>G
(DGKE)
MANE Select
|
NP_003638.1:p.Ala210=
|
|