ENST00000284061.8:c.999G=
(DGKE)
MANE Select
|
ENSP00000284061.3:p.Ala333=
|
|
ENST00000648772.1:c.*313+3137C=
(TRIM25)
|
ENSP00000498158.1:n.*313+3137C=
|
|
ENST00000284061.7:c.999G=
(DGKE)
|
ENSP00000284061.3:p.Ala333=
|
|
ENST00000572944.1:c.829G=
(DGKE)
|
|
|
NM_003647.2:c.999G=
(DGKE)
|
NP_003638.1:p.Ala333=
|
|
XM_011525394.1:c.1053G=
(DGKE)
|
XP_011523696.1:p.Ala351=
|
|
XM_011525395.1:c.1053G=
(DGKE)
|
XP_011523697.1:p.Ala351=
|
|
XM_011525396.1:c.1053G=
(DGKE)
|
XP_011523698.1:p.Ala351=
|
|
XM_011525397.1:c.1053G=
(DGKE)
|
XP_011523699.1:p.Ala351=
|
|
XM_011525398.1:c.543G=
(DGKE)
|
XP_011523700.1:p.Ala181=
|
|
XR_934581.1:n.1152G=
(DGKE)
|
|
|
XM_011525394.3:c.1053G=
(DGKE)
|
XP_011523696.1:p.Ala351=
|
|
XM_011525395.2:c.1053G=
(DGKE)
|
XP_011523697.1:p.Ala351=
|
|
XM_011525396.2:c.1053G=
(DGKE)
|
XP_011523698.1:p.Ala351=
|
|
XM_017025243.2:c.1371G=
(DGKE)
|
XP_016880732.1:p.Ala457=
|
|
XM_017025244.2:c.1053G=
(DGKE)
|
XP_016880733.1:p.Ala351=
|
|
XR_001752670.2:n.1557G=
(DGKE)
|
|
|
XR_001752671.1:n.1164G=
(DGKE)
|
|
|
XR_001752672.1:n.1165G=
(DGKE)
|
|
|
XR_002958079.1:n.1163G=
(DGKE)
|
|
|
NM_003647.3:c.999G=
(DGKE)
MANE Select
|
NP_003638.1:p.Ala333=
|
|