ENST00000697149.1:c.1568A>T
|
ENSP00000513138.1:n.1568A>T
|
|
ENST00000697150.1:c.1626A>T
|
ENSP00000513139.1:n.1626A>T
|
|
ENST00000697151.1:c.1559A>T
|
ENSP00000513140.1:n.1559A>T
|
|
ENST00000697164.1:c.1639A>T
|
ENSP00000513153.1:p.Asn547Tyr
|
|
ENST00000697165.1:c.1426A>T
|
ENSP00000513154.1:p.Asn476Tyr
|
|
ENST00000347310.10:c.1729A>T
MANE Select
|
ENSP00000321345.5:p.Asn577Tyr
|
|
ENST00000637002.1:c.1120A>T
|
ENSP00000490340.1:p.Asn374Tyr
|
|
ENST00000347310.9:c.1729A>T
|
ENSP00000321345.5:p.Asn577Tyr
|
|
ENST00000395227.2:c.523A>T
|
ENSP00000378652.2:p.Asn175Tyr
|
|
ENST00000425614.3:c.964A>T
|
ENSP00000387640.2:p.Asn322Tyr
|
|
ENST00000473881.2:c.*555A>T
|
ENSP00000486667.1:n.*555A>T
|
|
NM_144701.2:c.1729A>T
|
NP_653302.2:p.Asn577Tyr
|
|
XM_005270516.2:c.967A>T
|
XP_005270573.1:p.Asn323Tyr
|
|
XM_011540789.1:c.1819A>T
|
XP_011539091.1:p.Asn607Tyr
|
|
XM_011540790.1:c.1729A>T
|
XP_011539092.1:p.Asn577Tyr
|
|
XM_011540791.1:c.1729A>T
|
XP_011539093.1:p.Asn577Tyr
|
|
XM_011540790.3:c.1729A>T
|
XP_011539092.1:p.Asn577Tyr
|
|
XM_011540791.3:c.1729A>T
|
XP_011539093.1:p.Asn577Tyr
|
|
XR_001736993.1:n.1809A>T
|
|
|
NM_144701.3:c.1729A>T
MANE Select
|
NP_653302.2:p.Asn577Tyr
|
|