ENST00000697149.1:c.1453T>G
|
ENSP00000513138.1:n.1453T>G
|
|
ENST00000697150.1:c.1511T>G
|
ENSP00000513139.1:n.1511T>G
|
|
ENST00000697151.1:c.1444T>G
|
ENSP00000513140.1:n.1444T>G
|
|
ENST00000697164.1:c.1524T>G
|
ENSP00000513153.1:p.Asn508Lys
|
|
ENST00000697165.1:c.1311T>G
|
ENSP00000513154.1:p.Asn437Lys
|
|
ENST00000347310.10:c.1614T>G
MANE Select
|
ENSP00000321345.5:p.Asn538Lys
|
|
ENST00000637002.1:c.1005T>G
|
ENSP00000490340.1:p.Asn335Lys
|
|
ENST00000347310.9:c.1614T>G
|
ENSP00000321345.5:p.Asn538Lys
|
|
ENST00000395227.2:c.408T>G
|
ENSP00000378652.2:p.Asn136Lys
|
|
ENST00000425614.3:c.849T>G
|
ENSP00000387640.2:p.Asn283Lys
|
|
ENST00000473881.2:c.*440T>G
|
ENSP00000486667.1:n.*440T>G
|
|
NM_144701.2:c.1614T>G
|
NP_653302.2:p.Asn538Lys
|
|
XM_005270516.2:c.852T>G
|
XP_005270573.1:p.Asn284Lys
|
|
XM_011540789.1:c.1704T>G
|
XP_011539091.1:p.Asn568Lys
|
|
XM_011540790.1:c.1614T>G
|
XP_011539092.1:p.Asn538Lys
|
|
XM_011540791.1:c.1614T>G
|
XP_011539093.1:p.Asn538Lys
|
|
XM_011540790.3:c.1614T>G
|
XP_011539092.1:p.Asn538Lys
|
|
XM_011540791.3:c.1614T>G
|
XP_011539093.1:p.Asn538Lys
|
|
XR_001736993.1:n.1694T>G
|
|
|
NM_144701.3:c.1614T>G
MANE Select
|
NP_653302.2:p.Asn538Lys
|
|