ENST00000378823.8:c.2616T>A
MANE Select
|
ENSP00000368100.4:p.Ser872=
|
|
ENST00000638452.2:c.2319T>A
|
ENSP00000492349.2:p.Ser773=
|
|
ENST00000638504.1:n.2224T>A
|
|
|
ENST00000638568.2:c.2319T>A
|
ENSP00000491158.2:p.Ser773=
|
|
ENST00000639899.1:n.3135T>A
|
|
|
ENST00000640655.2:c.2319T>A
|
ENSP00000491596.2:p.Ser773=
|
|
ENST00000651160.1:c.*760T>A
|
ENSP00000498829.1:n.*760T>A
|
|
ENST00000651723.1:c.*2699T>A
|
ENSP00000498237.1:n.*2699T>A
|
|
ENST00000652016.1:c.*833T>A
|
ENSP00000498267.1:n.*833T>A
|
|
ENST00000652485.1:c.2649T>A
|
ENSP00000498973.1:p.Ser883=
|
|
ENST00000378823.7:c.2616T>A
|
ENSP00000368100.4:p.Ser872=
|
|
ENST00000423956.5:c.*802T>A
|
ENSP00000390971.1:n.*802T>A
|
|
ENST00000533482.5:c.*2242T>A
|
ENSP00000431225.1:n.*2242T>A
|
|
NM_005732.3:c.2616T>A
|
NP_005723.2:p.Ser872=
|
|
NM_005732.4:c.2616T>A
MANE Select
|
NP_005723.2:p.Ser872=
|
|