ENST00000378823.8:c.2595T>C
MANE Select
|
ENSP00000368100.4:p.Ser865=
|
|
ENST00000638452.2:c.2298T>C
|
ENSP00000492349.2:p.Ser766=
|
|
ENST00000638504.1:n.2203T>C
|
|
|
ENST00000638568.2:c.2298T>C
|
ENSP00000491158.2:p.Ser766=
|
|
ENST00000639899.1:n.3114T>C
|
|
|
ENST00000640655.2:c.2298T>C
|
ENSP00000491596.2:p.Ser766=
|
|
ENST00000651160.1:c.*739T>C
|
ENSP00000498829.1:n.*739T>C
|
|
ENST00000651723.1:c.*2678T>C
|
ENSP00000498237.1:n.*2678T>C
|
|
ENST00000652016.1:c.*812T>C
|
ENSP00000498267.1:n.*812T>C
|
|
ENST00000652485.1:c.2628T>C
|
ENSP00000498973.1:p.Ser876=
|
|
ENST00000378823.7:c.2595T>C
|
ENSP00000368100.4:p.Ser865=
|
|
ENST00000423956.5:c.*781T>C
|
ENSP00000390971.1:n.*781T>C
|
|
ENST00000533482.5:c.*2221T>C
|
ENSP00000431225.1:n.*2221T>C
|
|
NM_005732.3:c.2595T>C
|
NP_005723.2:p.Ser865=
|
|
NM_005732.4:c.2595T>C
MANE Select
|
NP_005723.2:p.Ser865=
|
|