ENST00000284061.8:c.981T>C
(DGKE)
MANE Select
|
ENSP00000284061.3:p.Ala327=
|
|
ENST00000648772.1:c.*313+3155A>G
(TRIM25)
|
ENSP00000498158.1:n.*313+3155A>G
|
|
ENST00000284061.7:c.981T>C
(DGKE)
|
ENSP00000284061.3:p.Ala327=
|
|
ENST00000572944.1:c.811T>C
(DGKE)
|
|
|
NM_003647.2:c.981T>C
(DGKE)
|
NP_003638.1:p.Ala327=
|
|
XM_011525394.1:c.1035T>C
(DGKE)
|
XP_011523696.1:p.Ala345=
|
|
XM_011525395.1:c.1035T>C
(DGKE)
|
XP_011523697.1:p.Ala345=
|
|
XM_011525396.1:c.1035T>C
(DGKE)
|
XP_011523698.1:p.Ala345=
|
|
XM_011525397.1:c.1035T>C
(DGKE)
|
XP_011523699.1:p.Ala345=
|
|
XM_011525398.1:c.525T>C
(DGKE)
|
XP_011523700.1:p.Ala175=
|
|
XR_934581.1:n.1134T>C
(DGKE)
|
|
|
XM_011525394.3:c.1035T>C
(DGKE)
|
XP_011523696.1:p.Ala345=
|
|
XM_011525395.2:c.1035T>C
(DGKE)
|
XP_011523697.1:p.Ala345=
|
|
XM_011525396.2:c.1035T>C
(DGKE)
|
XP_011523698.1:p.Ala345=
|
|
XM_017025243.2:c.1353T>C
(DGKE)
|
XP_016880732.1:p.Ala451=
|
|
XM_017025244.2:c.1035T>C
(DGKE)
|
XP_016880733.1:p.Ala345=
|
|
XR_001752670.2:n.1539T>C
(DGKE)
|
|
|
XR_001752671.1:n.1146T>C
(DGKE)
|
|
|
XR_001752672.1:n.1147T>C
(DGKE)
|
|
|
XR_002958079.1:n.1145T>C
(DGKE)
|
|
|
NM_003647.3:c.981T>C
(DGKE)
MANE Select
|
NP_003638.1:p.Ala327=
|
|