ENST00000379942.5:c.3567G>T
(PHKA2)
MANE Select
|
ENSP00000369274.4:p.Glu1189Asp
|
|
ENST00000379942.4:c.3567G>T
(PHKA2)
|
ENSP00000369274.4:p.Glu1189Asp
|
|
ENST00000469485.5:n.1292G>T
(PHKA2)
|
|
|
ENST00000473597.1:n.336G>T
(PHKA2)
|
|
|
ENST00000481718.1:n.2461G>T
(PHKA2)
|
|
|
NM_000292.2:c.3567G>T
(PHKA2)
|
NP_000283.1:p.Glu1189Asp
|
|
NR_029379.1:n.467+288C>A
(PHKA2-AS1)
|
|
|
XM_005274548.3:c.3513G>T
(PHKA2)
|
XP_005274605.1:p.Glu1171Asp
|
|
XM_005274550.3:c.3483G>T
(PHKA2)
|
XP_005274607.1:p.Glu1161Asp
|
|
XM_006724496.2:c.3591G>T
(PHKA2)
|
XP_006724559.1:p.Glu1197Asp
|
|
XM_006724498.2:c.3045G>T
(PHKA2)
|
XP_006724561.1:p.Glu1015Asp
|
|
XM_011545537.1:c.3492G>T
(PHKA2)
|
XP_011543839.1:p.Glu1164Asp
|
|
XM_011545538.1:c.2574G>T
(PHKA2)
|
XP_011543840.1:p.Glu858Asp
|
|
XM_005274548.5:c.3513G>T
(PHKA2)
|
XP_005274605.1:p.Glu1171Asp
|
|
XM_005274550.5:c.3483G>T
(PHKA2)
|
XP_005274607.1:p.Glu1161Asp
|
|
XM_006724496.4:c.3591G>T
(PHKA2)
|
XP_006724559.1:p.Glu1197Asp
|
|
XM_006724498.4:c.3045G>T
(PHKA2)
|
XP_006724561.1:p.Glu1015Asp
|
|
XM_011545537.3:c.3492G>T
(PHKA2)
|
XP_011543839.1:p.Glu1164Asp
|
|
XM_011545538.3:c.2574G>T
(PHKA2)
|
XP_011543840.1:p.Glu858Asp
|
|
XM_017029580.2:c.2685G>T
(PHKA2)
|
XP_016885069.1:p.Glu895Asp
|
|
XR_001755698.2:n.5695G>T
(PHKA2)
|
|
|
NM_000292.3:c.3567G>T
(PHKA2)
MANE Select
|
NP_000283.1:p.Glu1189Asp
|
|