ENST00000378823.8:c.1880A>T
MANE Select
|
ENSP00000368100.4:p.Asp627Val
|
|
ENST00000638452.2:c.1583A>T
|
ENSP00000492349.2:p.Asp528Val
|
|
ENST00000638504.1:n.1480-149A>T
|
|
|
ENST00000638568.2:c.1583A>T
|
ENSP00000491158.2:p.Asp528Val
|
|
ENST00000639899.1:n.2399A>T
|
|
|
ENST00000640655.2:c.1583A>T
|
ENSP00000491596.2:p.Asp528Val
|
|
ENST00000651160.1:c.*16-149A>T
|
ENSP00000498829.1:n.*16-149A>T
|
|
ENST00000651658.1:n.2423A>T
|
|
|
ENST00000651723.1:c.*1963A>T
|
ENSP00000498237.1:n.*1963A>T
|
|
ENST00000652016.1:c.*89-149A>T
|
ENSP00000498267.1:n.*89-149A>T
|
|
ENST00000652485.1:c.1913A>T
|
ENSP00000498973.1:p.Asp638Val
|
|
ENST00000378823.7:c.1880A>T
|
ENSP00000368100.4:p.Asp627Val
|
|
ENST00000423956.5:c.*66A>T
|
ENSP00000390971.1:n.*66A>T
|
|
ENST00000453394.5:c.1697A>T
|
ENSP00000400049.1:p.Asp566Val
|
|
ENST00000533482.5:c.*1506A>T
|
ENSP00000431225.1:n.*1506A>T
|
|
NM_005732.3:c.1880A>T
|
NP_005723.2:p.Asp627Val
|
|
NM_005732.4:c.1880A>T
MANE Select
|
NP_005723.2:p.Asp627Val
|
|