ENST00000697149.1:c.1497T>G
|
ENSP00000513138.1:n.1497T>G
|
|
ENST00000697150.1:c.1555T>G
|
ENSP00000513139.1:n.1555T>G
|
|
ENST00000697151.1:c.1488T>G
|
ENSP00000513140.1:n.1488T>G
|
|
ENST00000697164.1:c.1568T>G
|
ENSP00000513153.1:p.Leu523Ter
|
|
ENST00000697165.1:c.1355T>G
|
ENSP00000513154.1:p.Leu452Ter
|
|
ENST00000347310.10:c.1658T>G
MANE Select
|
ENSP00000321345.5:p.Leu553Ter
|
|
ENST00000637002.1:c.1049T>G
|
ENSP00000490340.1:p.Leu350Ter
|
|
ENST00000347310.9:c.1658T>G
|
ENSP00000321345.5:p.Leu553Ter
|
|
ENST00000395227.2:c.452T>G
|
ENSP00000378652.2:p.Leu151Ter
|
|
ENST00000425614.3:c.893T>G
|
ENSP00000387640.2:p.Leu298Ter
|
|
ENST00000473881.2:c.*484T>G
|
ENSP00000486667.1:n.*484T>G
|
|
NM_144701.2:c.1658T>G
|
NP_653302.2:p.Leu553Ter
|
|
XM_005270516.2:c.896T>G
|
XP_005270573.1:p.Leu299Ter
|
|
XM_011540789.1:c.1748T>G
|
XP_011539091.1:p.Leu583Ter
|
|
XM_011540790.1:c.1658T>G
|
XP_011539092.1:p.Leu553Ter
|
|
XM_011540791.1:c.1658T>G
|
XP_011539093.1:p.Leu553Ter
|
|
XM_011540790.3:c.1658T>G
|
XP_011539092.1:p.Leu553Ter
|
|
XM_011540791.3:c.1658T>G
|
XP_011539093.1:p.Leu553Ter
|
|
XR_001736993.1:n.1738T>G
|
|
|
NM_144701.3:c.1658T>G
MANE Select
|
NP_653302.2:p.Leu553Ter
|
|