ENST00000697149.1:c.1391T>G
|
ENSP00000513138.1:n.1391T>G
|
|
ENST00000697150.1:c.1449T>G
|
ENSP00000513139.1:n.1449T>G
|
|
ENST00000697151.1:c.1382T>G
|
ENSP00000513140.1:n.1382T>G
|
|
ENST00000697164.1:c.1462T>G
|
ENSP00000513153.1:p.Ser488Ala
|
|
ENST00000697165.1:c.1249T>G
|
ENSP00000513154.1:p.Ser417Ala
|
|
ENST00000347310.10:c.1552T>G
MANE Select
|
ENSP00000321345.5:p.Ser518Ala
|
|
ENST00000637002.1:c.943T>G
|
ENSP00000490340.1:p.Ser315Ala
|
|
ENST00000347310.9:c.1552T>G
|
ENSP00000321345.5:p.Ser518Ala
|
|
ENST00000395227.2:c.346T>G
|
ENSP00000378652.2:p.Ser116Ala
|
|
ENST00000425614.3:c.787T>G
|
ENSP00000387640.2:p.Ser263Ala
|
|
ENST00000473881.2:c.*378T>G
|
ENSP00000486667.1:n.*378T>G
|
|
NM_144701.2:c.1552T>G
|
NP_653302.2:p.Ser518Ala
|
|
XM_005270516.2:c.790T>G
|
XP_005270573.1:p.Ser264Ala
|
|
XM_011540789.1:c.1642T>G
|
XP_011539091.1:p.Ser548Ala
|
|
XM_011540790.1:c.1552T>G
|
XP_011539092.1:p.Ser518Ala
|
|
XM_011540791.1:c.1552T>G
|
XP_011539093.1:p.Ser518Ala
|
|
XM_011540790.3:c.1552T>G
|
XP_011539092.1:p.Ser518Ala
|
|
XM_011540791.3:c.1552T>G
|
XP_011539093.1:p.Ser518Ala
|
|
XR_001736993.1:n.1632T>G
|
|
|
NM_144701.3:c.1552T>G
MANE Select
|
NP_653302.2:p.Ser518Ala
|
|