ENST00000359526.9:c.1344A>C
MANE Select
|
ENSP00000352516.3:p.Glu448Asp
|
|
ENST00000676604.1:n.956A>C
|
|
|
ENST00000676610.1:c.1296A>C
|
ENSP00000504236.1:p.Glu432Asp
|
|
ENST00000676820.1:n.1352A>C
|
|
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ENST00000676868.1:n.1980A>C
|
|
|
ENST00000677013.1:c.*986A>C
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ENSP00000503135.1:n.*986A>C
|
|
ENST00000677250.1:c.*416A>C
|
ENSP00000502894.1:n.*416A>C
|
|
ENST00000677616.1:c.987A>C
|
ENSP00000503055.1:p.Glu329Asp
|
|
ENST00000677634.1:c.1296A>C
|
ENSP00000504246.1:p.Glu432Asp
|
|
ENST00000677685.1:c.*521A>C
|
ENSP00000503407.1:n.*521A>C
|
|
ENST00000677783.1:n.1766A>C
|
|
|
ENST00000677946.1:c.1296A>C
|
ENSP00000504202.1:p.Glu432Asp
|
|
ENST00000678024.1:n.1439A>C
|
|
|
ENST00000678694.1:n.617A>C
|
|
|
ENST00000678804.1:c.1296A>C
|
ENSP00000503853.1:p.Glu432Asp
|
|
ENST00000679103.1:c.1296A>C
|
ENSP00000503151.1:p.Glu432Asp
|
|
ENST00000679313.1:c.1296A>C
|
ENSP00000504512.1:p.Glu432Asp
|
|
ENST00000340748.8:c.1296A>C
|
ENSP00000345739.3:p.Glu432Asp
|
|
ENST00000359526.8:c.1344A>C
|
ENSP00000352516.3:p.Glu448Asp
|
|
ENST00000540357.5:c.288A>C
|
ENSP00000440457.2:p.Glu96Asp
|
|
ENST00000585843.1:n.501A>C
|
|
|
ENST00000592705.5:c.*1034A>C
|
ENSP00000466657.1:n.*1034A>C
|
|
NM_001130823.1:c.1344A>C , LRG_362t1:c.1344A>C
|
NP_001124295.1:p.Glu448Asp
|
|
NM_001379.2:c.1296A>C
|
NP_001370.1:p.Glu432Asp
|
|
XM_011527772.1:c.1344A>C
|
XP_011526074.1:p.Glu448Asp
|
|
XM_011527773.1:c.1296A>C
|
XP_011526075.1:p.Glu432Asp
|
|
XM_011527774.1:c.933A>C
|
XP_011526076.1:p.Glu311Asp
|
|
NM_001130823.2:c.1344A>C
|
NP_001124295.1:p.Glu448Asp
|
|
NM_001318730.1:c.1296A>C
|
NP_001305659.1:p.Glu432Asp
|
|
NM_001318731.1:c.981A>C
|
NP_001305660.1:p.Glu327Asp
|
|
NM_001379.3:c.1296A>C
|
NP_001370.1:p.Glu432Asp
|
|
NM_001130823.3:c.1344A>C
MANE Select
|
NP_001124295.1:p.Glu448Asp
|
|
NM_001318730.2:c.1296A>C
|
NP_001305659.1:p.Glu432Asp
|
|
NM_001318731.2:c.981A>C
|
NP_001305660.1:p.Glu327Asp
|
|
NM_001379.4:c.1296A>C
|
NP_001370.1:p.Glu432Asp
|
|