|
ENST00000485511.6:c.592G>A
(PPP2R5D)
MANE Select
|
ENSP00000417963.1:p.Glu198Lys
|
|
|
ENST00000676174.1:n.251G>A
(PPP2R5D)
|
|
|
|
ENST00000230402.10:c.*273G>A
(PPP2R5D)
|
ENSP00000230402.6:n.*273G>A
|
|
|
ENST00000394110.7:c.496G>A
(PPP2R5D)
|
ENSP00000377669.3:p.Glu166Lys
|
|
|
ENST00000461010.5:c.274G>A
(PPP2R5D)
|
ENSP00000420674.1:p.Glu92Lys
|
|
|
ENST00000467447.1:n.169G>A
(PPP2R5D)
|
|
|
|
ENST00000470467.5:c.350G>A
(PPP2R5D)
|
|
|
|
ENST00000472118.5:c.568G>A
(PPP2R5D)
|
ENSP00000420550.1:p.Glu190Lys
|
|
|
ENST00000485511.5:c.592G>A
(PPP2R5D)
|
ENSP00000417963.1:p.Glu198Lys
|
|
|
NM_001270476.1:c.139G>A
(PPP2R5D)
|
NP_001257405.1:p.Glu47Lys
|
|
|
NM_006245.3:c.592G>A
(PPP2R5D)
|
NP_006236.1:p.Glu198Lys
|
|
|
NM_180976.2:c.496G>A
(PPP2R5D)
|
NP_851307.1:p.Glu166Lys
|
|
|
NM_180977.2:c.274G>A
(PPP2R5D)
|
NP_851308.1:p.Glu92Lys
|
|
|
XM_005249123.1:c.367+5661C>T
(MEA1)
|
XP_005249180.1:n.367+5661C>T
|
|
|
XM_017010868.1:c.367+5661C>T
(MEA1)
|
XP_016866357.1:n.367+5661C>T
|
|
|
NM_006245.4:c.592G>A
(PPP2R5D)
MANE Select
|
NP_006236.1:p.Glu198Lys
|
|
|
NM_001270476.2:c.139G>A
(PPP2R5D)
|
NP_001257405.1:p.Glu47Lys
|
|
|
NM_180976.3:c.496G>A
(PPP2R5D)
|
NP_851307.1:p.Glu166Lys
|
|
|
NM_180977.3:c.274G>A
(PPP2R5D)
|
NP_851308.1:p.Glu92Lys
|
|
