ENST00000469280.2:n.778T>A
(NCF2)
|
|
|
ENST00000697329.1:n.1258T>A
(NCF2)
|
|
|
ENST00000697330.1:c.1338T>A
(NCF2)
|
ENSP00000513258.1:p.Asp446Glu
|
|
ENST00000697351.1:c.1230T>A
(NCF2)
|
ENSP00000513276.1:p.Asp410Glu
|
|
ENST00000367535.8:c.1338T>A
(NCF2)
MANE Select
|
ENSP00000356505.4:p.Asp446Glu
|
|
ENST00000367535.7:c.1338T>A
(NCF2)
|
ENSP00000356505.3:p.Asp446Glu
|
|
ENST00000367536.5:c.1338T>A
(NCF2)
|
ENSP00000356506.1:p.Asp446Glu
|
|
ENST00000413720.5:c.1203T>A
(NCF2)
|
ENSP00000399294.1:p.Asp401Glu
|
|
ENST00000418089.5:c.1095T>A
(NCF2)
|
ENSP00000407217.1:p.Asp365Glu
|
|
ENST00000495321.1:n.233+9036A>T
(SMG7)
|
|
|
NM_000433.3:c.1338T>A , LRG_88t1:c.1338T>A
(NCF2)
|
NP_000424.2:p.Asp446Glu
|
|
NM_001127651.2:c.1338T>A
(NCF2)
|
NP_001121123.1:p.Asp446Glu
|
|
NM_001190789.1:c.1095T>A
(NCF2)
|
NP_001177718.1:p.Asp365Glu
|
|
NM_001190794.1:c.1203T>A
(NCF2)
|
NP_001177723.1:p.Asp401Glu
|
|
XM_005245207.1:c.1230T>A
(NCF2)
|
XP_005245264.1:p.Asp410Glu
|
|
XM_011509580.1:c.1338T>A
(NCF2)
|
XP_011507882.1:p.Asp446Glu
|
|
XM_011509581.1:c.1338T>A
(NCF2)
|
XP_011507883.1:p.Asp446Glu
|
|
NM_000433.4:c.1338T>A
(NCF2)
MANE Select
|
NP_000424.2:p.Asp446Glu
|
|
NM_001127651.3:c.1338T>A
(NCF2)
|
NP_001121123.1:p.Asp446Glu
|
|
NM_001190789.2:c.1095T>A
(NCF2)
|
NP_001177718.1:p.Asp365Glu
|
|
NM_001190794.2:c.1203T>A
(NCF2)
|
NP_001177723.1:p.Asp401Glu
|
|