ENST00000378823.8:c.2649T>G
MANE Select
|
ENSP00000368100.4:p.Arg883=
|
|
ENST00000638452.2:c.2352T>G
|
ENSP00000492349.2:p.Arg784=
|
|
ENST00000638504.1:n.2257T>G
|
|
|
ENST00000638568.2:c.2352T>G
|
ENSP00000491158.2:p.Arg784=
|
|
ENST00000639899.1:n.3168T>G
|
|
|
ENST00000640655.2:c.2352T>G
|
ENSP00000491596.2:p.Arg784=
|
|
ENST00000651160.1:c.*793T>G
|
ENSP00000498829.1:n.*793T>G
|
|
ENST00000651723.1:c.*2732T>G
|
ENSP00000498237.1:n.*2732T>G
|
|
ENST00000652016.1:c.*866T>G
|
ENSP00000498267.1:n.*866T>G
|
|
ENST00000652485.1:c.2682T>G
|
ENSP00000498973.1:p.Arg894=
|
|
ENST00000378823.7:c.2649T>G
|
ENSP00000368100.4:p.Arg883=
|
|
ENST00000423956.5:c.*835T>G
|
ENSP00000390971.1:n.*835T>G
|
|
ENST00000533482.5:c.*2275T>G
|
ENSP00000431225.1:n.*2275T>G
|
|
NM_005732.3:c.2649T>G
|
NP_005723.2:p.Arg883=
|
|
NM_005732.4:c.2649T>G
MANE Select
|
NP_005723.2:p.Arg883=
|
|