ENST00000697149.1:c.1424A>G
|
ENSP00000513138.1:n.1424A>G
|
|
ENST00000697150.1:c.1482A>G
|
ENSP00000513139.1:n.1482A>G
|
|
ENST00000697151.1:c.1415A>G
|
ENSP00000513140.1:n.1415A>G
|
|
ENST00000697164.1:c.1495A>G
|
ENSP00000513153.1:p.Asn499Asp
|
|
ENST00000697165.1:c.1282A>G
|
ENSP00000513154.1:p.Asn428Asp
|
|
ENST00000347310.10:c.1585A>G
MANE Select
|
ENSP00000321345.5:p.Asn529Asp
|
|
ENST00000637002.1:c.976A>G
|
ENSP00000490340.1:p.Asn326Asp
|
|
ENST00000347310.9:c.1585A>G
|
ENSP00000321345.5:p.Asn529Asp
|
|
ENST00000395227.2:c.379A>G
|
ENSP00000378652.2:p.Asn127Asp
|
|
ENST00000425614.3:c.820A>G
|
ENSP00000387640.2:p.Asn274Asp
|
|
ENST00000473881.2:c.*411A>G
|
ENSP00000486667.1:n.*411A>G
|
|
NM_144701.2:c.1585A>G
|
NP_653302.2:p.Asn529Asp
|
|
XM_005270516.2:c.823A>G
|
XP_005270573.1:p.Asn275Asp
|
|
XM_011540789.1:c.1675A>G
|
XP_011539091.1:p.Asn559Asp
|
|
XM_011540790.1:c.1585A>G
|
XP_011539092.1:p.Asn529Asp
|
|
XM_011540791.1:c.1585A>G
|
XP_011539093.1:p.Asn529Asp
|
|
XM_011540790.3:c.1585A>G
|
XP_011539092.1:p.Asn529Asp
|
|
XM_011540791.3:c.1585A>G
|
XP_011539093.1:p.Asn529Asp
|
|
XR_001736993.1:n.1665A>G
|
|
|
NM_144701.3:c.1585A>G
MANE Select
|
NP_653302.2:p.Asn529Asp
|
|