ENST00000379942.5:c.3549T>G
(PHKA2)
MANE Select
|
ENSP00000369274.4:p.Gly1183=
|
|
ENST00000379942.4:c.3549T>G
(PHKA2)
|
ENSP00000369274.4:p.Gly1183=
|
|
ENST00000469485.5:n.1274T>G
(PHKA2)
|
|
|
ENST00000473597.1:n.318T>G
(PHKA2)
|
|
|
ENST00000481718.1:n.2443T>G
(PHKA2)
|
|
|
NM_000292.2:c.3549T>G
(PHKA2)
|
NP_000283.1:p.Gly1183=
|
|
NR_029379.1:n.467+306A>C
(PHKA2-AS1)
|
|
|
XM_005274548.3:c.3495T>G
(PHKA2)
|
XP_005274605.1:p.Gly1165=
|
|
XM_005274550.3:c.3465T>G
(PHKA2)
|
XP_005274607.1:p.Gly1155=
|
|
XM_006724496.2:c.3573T>G
(PHKA2)
|
XP_006724559.1:p.Gly1191=
|
|
XM_006724498.2:c.3027T>G
(PHKA2)
|
XP_006724561.1:p.Gly1009=
|
|
XM_011545537.1:c.3474T>G
(PHKA2)
|
XP_011543839.1:p.Gly1158=
|
|
XM_011545538.1:c.2556T>G
(PHKA2)
|
XP_011543840.1:p.Gly852=
|
|
XM_005274548.5:c.3495T>G
(PHKA2)
|
XP_005274605.1:p.Gly1165=
|
|
XM_005274550.5:c.3465T>G
(PHKA2)
|
XP_005274607.1:p.Gly1155=
|
|
XM_006724496.4:c.3573T>G
(PHKA2)
|
XP_006724559.1:p.Gly1191=
|
|
XM_006724498.4:c.3027T>G
(PHKA2)
|
XP_006724561.1:p.Gly1009=
|
|
XM_011545537.3:c.3474T>G
(PHKA2)
|
XP_011543839.1:p.Gly1158=
|
|
XM_011545538.3:c.2556T>G
(PHKA2)
|
XP_011543840.1:p.Gly852=
|
|
XM_017029580.2:c.2667T>G
(PHKA2)
|
XP_016885069.1:p.Gly889=
|
|
XR_001755698.2:n.5677T>G
(PHKA2)
|
|
|
NM_000292.3:c.3549T>G
(PHKA2)
MANE Select
|
NP_000283.1:p.Gly1183=
|
|