ENST00000378823.8:c.1880A=
MANE Select
|
ENSP00000368100.4:p.Asp627=
|
|
ENST00000638452.2:c.1583A=
|
ENSP00000492349.2:p.Asp528=
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|
ENST00000638504.1:n.1480-149A=
|
|
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ENST00000638568.2:c.1583A=
|
ENSP00000491158.2:p.Asp528=
|
|
ENST00000639899.1:n.2399A=
|
|
|
ENST00000640655.2:c.1583A=
|
ENSP00000491596.2:p.Asp528=
|
|
ENST00000651160.1:c.*16-149A=
|
ENSP00000498829.1:n.*16-149A=
|
|
ENST00000651658.1:n.2423A=
|
|
|
ENST00000651723.1:c.*1963A=
|
ENSP00000498237.1:n.*1963A=
|
|
ENST00000652016.1:c.*89-149A=
|
ENSP00000498267.1:n.*89-149A=
|
|
ENST00000652485.1:c.1913A=
|
ENSP00000498973.1:p.Asp638=
|
|
ENST00000378823.7:c.1880A=
|
ENSP00000368100.4:p.Asp627=
|
|
ENST00000423956.5:c.*66A=
|
ENSP00000390971.1:n.*66A=
|
|
ENST00000453394.5:c.1697A=
|
ENSP00000400049.1:p.Asp566=
|
|
ENST00000533482.5:c.*1506A=
|
ENSP00000431225.1:n.*1506A=
|
|
NM_005732.3:c.1880A=
|
NP_005723.2:p.Asp627=
|
|
NM_005732.4:c.1880A=
MANE Select
|
NP_005723.2:p.Asp627=
|
|