ENST00000379942.5:c.3595T>G
(PHKA2)
MANE Select
|
ENSP00000369274.4:p.Phe1199Val
|
|
ENST00000379942.4:c.3595T>G
(PHKA2)
|
ENSP00000369274.4:p.Phe1199Val
|
|
ENST00000469485.5:n.1320T>G
(PHKA2)
|
|
|
ENST00000473597.1:n.364T>G
(PHKA2)
|
|
|
ENST00000481718.1:n.2489T>G
(PHKA2)
|
|
|
NM_000292.2:c.3595T>G
(PHKA2)
|
NP_000283.1:p.Phe1199Val
|
|
NR_029379.1:n.467+260A>C
(PHKA2-AS1)
|
|
|
XM_005274548.3:c.3541T>G
(PHKA2)
|
XP_005274605.1:p.Phe1181Val
|
|
XM_005274550.3:c.3511T>G
(PHKA2)
|
XP_005274607.1:p.Phe1171Val
|
|
XM_006724496.2:c.3619T>G
(PHKA2)
|
XP_006724559.1:p.Phe1207Val
|
|
XM_006724498.2:c.3073T>G
(PHKA2)
|
XP_006724561.1:p.Phe1025Val
|
|
XM_011545537.1:c.3520T>G
(PHKA2)
|
XP_011543839.1:p.Phe1174Val
|
|
XM_011545538.1:c.2602T>G
(PHKA2)
|
XP_011543840.1:p.Phe868Val
|
|
XM_005274548.5:c.3541T>G
(PHKA2)
|
XP_005274605.1:p.Phe1181Val
|
|
XM_005274550.5:c.3511T>G
(PHKA2)
|
XP_005274607.1:p.Phe1171Val
|
|
XM_006724496.4:c.3619T>G
(PHKA2)
|
XP_006724559.1:p.Phe1207Val
|
|
XM_006724498.4:c.3073T>G
(PHKA2)
|
XP_006724561.1:p.Phe1025Val
|
|
XM_011545537.3:c.3520T>G
(PHKA2)
|
XP_011543839.1:p.Phe1174Val
|
|
XM_011545538.3:c.2602T>G
(PHKA2)
|
XP_011543840.1:p.Phe868Val
|
|
XM_017029580.2:c.2713T>G
(PHKA2)
|
XP_016885069.1:p.Phe905Val
|
|
XR_001755698.2:n.5723T>G
(PHKA2)
|
|
|
NM_000292.3:c.3595T>G
(PHKA2)
MANE Select
|
NP_000283.1:p.Phe1199Val
|
|