ENST00000497571.6:c.260A>T
MANE Select
|
ENSP00000419923.1:p.Glu87Val
|
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ENST00000380946.3:n.495A>T
|
|
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ENST00000469435.1:c.260A>T
|
ENSP00000419079.1:p.Glu87Val
|
|
ENST00000497571.5:c.260A>T
|
ENSP00000419923.1:p.Glu87Val
|
|
ENST00000542957.1:c.260A>T
|
ENSP00000445301.1:p.Glu87Val
|
|
NM_001160124.1:c.260A>T
|
NP_001153596.1:p.Glu87Val
|
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NM_001160125.1:c.260A>T
|
NP_001153597.1:p.Glu87Val
|
|
NM_001300.5:c.260A>T
|
NP_001291.3:p.Glu87Val
|
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NR_027653.1:n.527A>T
|
|
|
NM_001300.6:c.260A>T
MANE Select
|
NP_001291.3:p.Glu87Val
|
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NM_001160124.2:c.260A>T
|
NP_001153596.1:p.Glu87Val
|
|
NR_027653.2:n.455A>T
|
|
|
NM_001160125.2:c.260A>T
|
NP_001153597.1:p.Glu87Val
|
|