ENST00000378823.8:c.1812T>G
MANE Select
|
ENSP00000368100.4:p.Ser604=
|
|
ENST00000638452.2:c.1515T>G
|
ENSP00000492349.2:p.Ser505=
|
|
ENST00000638504.1:n.1480-217T>G
|
|
|
ENST00000638568.2:c.1515T>G
|
ENSP00000491158.2:p.Ser505=
|
|
ENST00000639899.1:n.2331T>G
|
|
|
ENST00000640655.2:c.1515T>G
|
ENSP00000491596.2:p.Ser505=
|
|
ENST00000651160.1:c.*16-217T>G
|
ENSP00000498829.1:n.*16-217T>G
|
|
ENST00000651658.1:n.2355T>G
|
|
|
ENST00000651723.1:c.*1895T>G
|
ENSP00000498237.1:n.*1895T>G
|
|
ENST00000652016.1:c.*88+210T>G
|
ENSP00000498267.1:n.*88+210T>G
|
|
ENST00000652485.1:c.1845T>G
|
ENSP00000498973.1:p.Ser615=
|
|
ENST00000378823.7:c.1812T>G
|
ENSP00000368100.4:p.Ser604=
|
|
ENST00000423956.5:c.1654T>G
|
ENSP00000390971.1:p.Ter552Gly
|
|
ENST00000453394.5:c.1629T>G
|
ENSP00000400049.1:p.Ser543=
|
|
ENST00000533482.5:c.*1438T>G
|
ENSP00000431225.1:n.*1438T>G
|
|
NM_005732.3:c.1812T>G
|
NP_005723.2:p.Ser604=
|
|
NM_005732.4:c.1812T>G
MANE Select
|
NP_005723.2:p.Ser604=
|
|