ENST00000485511.6:c.1258G>A
(PPP2R5D)
MANE Select
|
ENSP00000417963.1:p.Glu420Lys
|
|
ENST00000676174.1:n.1579G>A
(PPP2R5D)
|
|
|
ENST00000230402.10:c.*939G>A
(PPP2R5D)
|
ENSP00000230402.6:n.*939G>A
|
|
ENST00000394110.7:c.1162G>A
(PPP2R5D)
|
ENSP00000377669.3:p.Glu388Lys
|
|
ENST00000461010.5:c.940G>A
(PPP2R5D)
|
ENSP00000420674.1:p.Glu314Lys
|
|
ENST00000470467.5:c.962G>A
(PPP2R5D)
|
|
|
ENST00000472118.5:c.1234G>A
(PPP2R5D)
|
ENSP00000420550.1:p.Glu412Lys
|
|
ENST00000482315.1:n.429G>A
(PPP2R5D)
|
|
|
ENST00000485511.5:c.1258G>A
(PPP2R5D)
|
ENSP00000417963.1:p.Glu420Lys
|
|
ENST00000486843.1:c.122G>A
(PPP2R5D)
|
|
|
NM_001270476.1:c.805G>A
(PPP2R5D)
|
NP_001257405.1:p.Glu269Lys
|
|
NM_006245.3:c.1258G>A
(PPP2R5D)
|
NP_006236.1:p.Glu420Lys
|
|
NM_180976.2:c.1162G>A
(PPP2R5D)
|
NP_851307.1:p.Glu388Lys
|
|
NM_180977.2:c.940G>A
(PPP2R5D)
|
NP_851308.1:p.Glu314Lys
|
|
XM_005249123.1:c.367+3598C>T
(MEA1)
|
XP_005249180.1:n.367+3598C>T
|
|
XM_017010868.1:c.367+3598C>T
(MEA1)
|
XP_016866357.1:n.367+3598C>T
|
|
NM_006245.4:c.1258G>A
(PPP2R5D)
MANE Select
|
NP_006236.1:p.Glu420Lys
|
|
NM_001270476.2:c.805G>A
(PPP2R5D)
|
NP_001257405.1:p.Glu269Lys
|
|
NM_180976.3:c.1162G>A
(PPP2R5D)
|
NP_851307.1:p.Glu388Lys
|
|
NM_180977.3:c.940G>A
(PPP2R5D)
|
NP_851308.1:p.Glu314Lys
|
|