ENST00000290866.10:c.3651G>A
MANE Select
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ENSP00000290866.4:p.Glu1217=
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ENST00000290863.10:c.1929G>A
|
ENSP00000290863.6:p.Glu643=
|
|
ENST00000290866.9:c.3651G>A
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ENSP00000290866.4:p.Glu1217=
|
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ENST00000413513.7:c.1806G>A
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ENSP00000392247.3:p.Glu602=
|
|
ENST00000428043.5:c.3651G>A
|
ENSP00000397593.2:p.Glu1217=
|
|
ENST00000577418.5:n.661G>A
|
|
|
ENST00000577647.2:c.1929G>A
|
ENSP00000464149.1:p.Glu643=
|
|
ENST00000578839.5:c.*1406G>A
|
ENSP00000462110.2:n.*1406G>A
|
|
ENST00000579314.5:c.*1380G>A
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ENSP00000462599.1:n.*1380G>A
|
|
ENST00000579409.1:c.338G>A
|
|
|
ENST00000582244.1:n.525G>A
|
|
|
NM_000789.3:c.3651G>A
|
NP_000780.1:p.Glu1217=
|
|
NM_001178057.1:c.1806G>A
|
NP_001171528.1:p.Glu602=
|
|
NM_152830.2:c.1929G>A
|
NP_690043.1:p.Glu643=
|
|
XM_005257110.1:c.3102G>A
|
XP_005257167.1:p.Glu1034=
|
|
XM_006721737.2:c.1989G>A
|
XP_006721800.2:p.Glu663=
|
|
XM_006721737.3:c.1989G>A
|
XP_006721800.2:p.Glu663=
|
|
NM_000789.4:c.3651G>A
MANE Select
|
NP_000780.1:p.Glu1217=
|
|
NM_001178057.2:c.1806G>A
|
NP_001171528.1:p.Glu602=
|
|
NM_152830.3:c.1929G>A
|
NP_690043.1:p.Glu643=
|
|
NM_001382700.1:c.3084G>A
|
NP_001369629.1:p.Glu1028=
|
|
NM_001382701.1:c.2799G>A
|
NP_001369630.1:p.Glu933=
|
|
NM_001382702.1:c.1266G>A
|
NP_001369631.1:p.Glu422=
|
|
NR_168483.1:n.2029G>A
|
|
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