ENST00000274576.9:c.294C>A
MANE Select
|
ENSP00000274576.5:p.Asp98Glu
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ENST00000274576.8:c.294C>A
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ENSP00000274576.4:p.Asp98Glu
|
|
ENST00000455880.2:c.294C>A
|
ENSP00000411593.2:p.Asp98Glu
|
|
ENST00000462581.6:c.*52C>A
|
ENSP00000430595.1:n.*52C>A
|
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ENST00000471351.2:n.577C>A
|
|
|
NM_000171.3:c.294C>A
|
NP_000162.2:p.Asp98Glu
|
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NM_001146040.1:c.294C>A
|
NP_001139512.1:p.Asp98Glu
|
|
NM_001292000.1:c.45C>A
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NP_001278929.1:p.Asp15Glu
|
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XM_005268412.2:c.294C>A
|
XP_005268469.1:p.Asp98Glu
|
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XR_002956230.1:n.229+2074G>T
|
|
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NM_000171.4:c.294C>A
MANE Select
|
NP_000162.2:p.Asp98Glu
|
|
NM_001146040.2:c.294C>A
|
NP_001139512.1:p.Asp98Glu
|
|
NM_001292000.2:c.45C>A
|
NP_001278929.1:p.Asp15Glu
|
|