ENST00000697149.1:c.1560T>G
|
ENSP00000513138.1:n.1560T>G
|
|
ENST00000697150.1:c.1618T>G
|
ENSP00000513139.1:n.1618T>G
|
|
ENST00000697151.1:c.1551T>G
|
ENSP00000513140.1:n.1551T>G
|
|
ENST00000697164.1:c.1631T>G
|
ENSP00000513153.1:p.Leu544Arg
|
|
ENST00000697165.1:c.1418T>G
|
ENSP00000513154.1:p.Leu473Arg
|
|
ENST00000347310.10:c.1721T>G
MANE Select
|
ENSP00000321345.5:p.Leu574Arg
|
|
ENST00000637002.1:c.1112T>G
|
ENSP00000490340.1:p.Leu371Arg
|
|
ENST00000347310.9:c.1721T>G
|
ENSP00000321345.5:p.Leu574Arg
|
|
ENST00000395227.2:c.515T>G
|
ENSP00000378652.2:p.Leu172Arg
|
|
ENST00000425614.3:c.956T>G
|
ENSP00000387640.2:p.Leu319Arg
|
|
ENST00000473881.2:c.*547T>G
|
ENSP00000486667.1:n.*547T>G
|
|
NM_144701.2:c.1721T>G
|
NP_653302.2:p.Leu574Arg
|
|
XM_005270516.2:c.959T>G
|
XP_005270573.1:p.Leu320Arg
|
|
XM_011540789.1:c.1811T>G
|
XP_011539091.1:p.Leu604Arg
|
|
XM_011540790.1:c.1721T>G
|
XP_011539092.1:p.Leu574Arg
|
|
XM_011540791.1:c.1721T>G
|
XP_011539093.1:p.Leu574Arg
|
|
XM_011540790.3:c.1721T>G
|
XP_011539092.1:p.Leu574Arg
|
|
XM_011540791.3:c.1721T>G
|
XP_011539093.1:p.Leu574Arg
|
|
XR_001736993.1:n.1801T>G
|
|
|
NM_144701.3:c.1721T>G
MANE Select
|
NP_653302.2:p.Leu574Arg
|
|