ENST00000697149.1:c.1463A>G
|
ENSP00000513138.1:n.1463A>G
|
|
ENST00000697150.1:c.1521A>G
|
ENSP00000513139.1:n.1521A>G
|
|
ENST00000697151.1:c.1454A>G
|
ENSP00000513140.1:n.1454A>G
|
|
ENST00000697164.1:c.1534A>G
|
ENSP00000513153.1:p.Asn512Asp
|
|
ENST00000697165.1:c.1321A>G
|
ENSP00000513154.1:p.Asn441Asp
|
|
ENST00000347310.10:c.1624A>G
MANE Select
|
ENSP00000321345.5:p.Asn542Asp
|
|
ENST00000637002.1:c.1015A>G
|
ENSP00000490340.1:p.Asn339Asp
|
|
ENST00000347310.9:c.1624A>G
|
ENSP00000321345.5:p.Asn542Asp
|
|
ENST00000395227.2:c.418A>G
|
ENSP00000378652.2:p.Asn140Asp
|
|
ENST00000425614.3:c.859A>G
|
ENSP00000387640.2:p.Asn287Asp
|
|
ENST00000473881.2:c.*450A>G
|
ENSP00000486667.1:n.*450A>G
|
|
NM_144701.2:c.1624A>G
|
NP_653302.2:p.Asn542Asp
|
|
XM_005270516.2:c.862A>G
|
XP_005270573.1:p.Asn288Asp
|
|
XM_011540789.1:c.1714A>G
|
XP_011539091.1:p.Asn572Asp
|
|
XM_011540790.1:c.1624A>G
|
XP_011539092.1:p.Asn542Asp
|
|
XM_011540791.1:c.1624A>G
|
XP_011539093.1:p.Asn542Asp
|
|
XM_011540790.3:c.1624A>G
|
XP_011539092.1:p.Asn542Asp
|
|
XM_011540791.3:c.1624A>G
|
XP_011539093.1:p.Asn542Asp
|
|
XR_001736993.1:n.1704A>G
|
|
|
NM_144701.3:c.1624A>G
MANE Select
|
NP_653302.2:p.Asn542Asp
|
|