ENST00000697149.1:c.1670T>G
|
ENSP00000513138.1:n.1670T>G
|
|
ENST00000697150.1:c.1728T>G
|
ENSP00000513139.1:n.1728T>G
|
|
ENST00000697151.1:c.1661T>G
|
ENSP00000513140.1:n.1661T>G
|
|
ENST00000697164.1:c.1741T>G
|
ENSP00000513153.1:p.Tyr581Asp
|
|
ENST00000697165.1:c.1528T>G
|
ENSP00000513154.1:p.Tyr510Asp
|
|
ENST00000347310.10:c.1831T>G
MANE Select
|
ENSP00000321345.5:p.Tyr611Asp
|
|
ENST00000637002.1:c.1222T>G
|
ENSP00000490340.1:p.Tyr408Asp
|
|
ENST00000347310.9:c.1831T>G
|
ENSP00000321345.5:p.Tyr611Asp
|
|
ENST00000395227.2:c.625T>G
|
ENSP00000378652.2:p.Tyr209Asp
|
|
ENST00000425614.3:c.1066T>G
|
ENSP00000387640.2:p.Tyr356Asp
|
|
ENST00000473881.2:c.*657T>G
|
ENSP00000486667.1:n.*657T>G
|
|
NM_144701.2:c.1831T>G
|
NP_653302.2:p.Tyr611Asp
|
|
XM_005270516.2:c.1069T>G
|
XP_005270573.1:p.Tyr357Asp
|
|
XM_011540789.1:c.1921T>G
|
XP_011539091.1:p.Tyr641Asp
|
|
XM_011540790.1:c.1831T>G
|
XP_011539092.1:p.Tyr611Asp
|
|
XM_011540791.1:c.1831T>G
|
XP_011539093.1:p.Tyr611Asp
|
|
XM_011540790.3:c.1831T>G
|
XP_011539092.1:p.Tyr611Asp
|
|
XM_011540791.3:c.1831T>G
|
XP_011539093.1:p.Tyr611Asp
|
|
XR_001736993.1:n.1911T>G
|
|
|
NM_144701.3:c.1831T>G
MANE Select
|
NP_653302.2:p.Tyr611Asp
|
|