ENST00000378823.8:c.2527T>G
MANE Select
|
ENSP00000368100.4:p.Ser843Ala
|
|
ENST00000638452.2:c.2230T>G
|
ENSP00000492349.2:p.Ser744Ala
|
|
ENST00000638504.1:n.2135T>G
|
|
|
ENST00000638568.2:c.2230T>G
|
ENSP00000491158.2:p.Ser744Ala
|
|
ENST00000639899.1:n.3046T>G
|
|
|
ENST00000640655.2:c.2230T>G
|
ENSP00000491596.2:p.Ser744Ala
|
|
ENST00000651160.1:c.*671T>G
|
ENSP00000498829.1:n.*671T>G
|
|
ENST00000651723.1:c.*2610T>G
|
ENSP00000498237.1:n.*2610T>G
|
|
ENST00000652016.1:c.*744T>G
|
ENSP00000498267.1:n.*744T>G
|
|
ENST00000652485.1:c.2560T>G
|
ENSP00000498973.1:p.Ser854Ala
|
|
ENST00000378823.7:c.2527T>G
|
ENSP00000368100.4:p.Ser843Ala
|
|
ENST00000423956.5:c.*713T>G
|
ENSP00000390971.1:n.*713T>G
|
|
ENST00000533482.5:c.*2153T>G
|
ENSP00000431225.1:n.*2153T>G
|
|
NM_005732.3:c.2527T>G
|
NP_005723.2:p.Ser843Ala
|
|
NM_005732.4:c.2527T>G
MANE Select
|
NP_005723.2:p.Ser843Ala
|
|