ENST00000263038.9:c.753G>T
MANE Select
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ENSP00000263038.4:p.Glu251Asp
|
|
ENST00000263038.8:c.753G>T
|
ENSP00000263038.4:p.Glu251Asp
|
|
ENST00000396913.6:c.453G>T
|
ENSP00000380121.2:p.Glu151Asp
|
|
ENST00000396920.7:c.702G>T
|
ENSP00000380126.3:p.Glu234Asp
|
|
ENST00000453759.6:c.453G>T
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ENSP00000412525.2:p.Glu151Asp
|
|
NM_001037537.1:c.453G>T
|
NP_001032626.1:p.Glu151Asp
|
|
NM_006214.3:c.753G>T
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NP_006205.1:p.Glu251Asp
|
|
XM_005252469.2:c.534G>T
|
XP_005252526.1:p.Glu178Asp
|
|
NM_001323080.1:c.453G>T
|
NP_001310009.1:p.Glu151Asp
|
|
NM_001323082.1:c.759G>T
|
NP_001310011.1:p.Glu253Asp
|
|
NM_001323083.1:c.489G>T
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NP_001310012.1:p.Glu163Asp
|
|
NM_001323084.1:c.459G>T
|
NP_001310013.1:p.Glu153Asp
|
|
NM_006214.4:c.753G>T
MANE Select
|
NP_006205.1:p.Glu251Asp
|
|
NM_001037537.2:c.453G>T
|
NP_001032626.1:p.Glu151Asp
|
|
NM_001323080.2:c.453G>T
|
NP_001310009.1:p.Glu151Asp
|
|
NM_001323082.2:c.759G>T
|
NP_001310011.1:p.Glu253Asp
|
|
NM_001323083.2:c.489G>T
|
NP_001310012.1:p.Glu163Asp
|
|
NM_001323084.2:c.459G>T
|
NP_001310013.1:p.Glu153Asp
|
|