ENST00000697149.1:c.1503A>G
|
ENSP00000513138.1:n.1503A>G
|
|
ENST00000697150.1:c.1561A>G
|
ENSP00000513139.1:n.1561A>G
|
|
ENST00000697151.1:c.1494A>G
|
ENSP00000513140.1:n.1494A>G
|
|
ENST00000697164.1:c.1574A>G
|
ENSP00000513153.1:p.Gln525Arg
|
|
ENST00000697165.1:c.1361A>G
|
ENSP00000513154.1:p.Gln454Arg
|
|
ENST00000347310.10:c.1664A>G
MANE Select
|
ENSP00000321345.5:p.Gln555Arg
|
|
ENST00000637002.1:c.1055A>G
|
ENSP00000490340.1:p.Gln352Arg
|
|
ENST00000347310.9:c.1664A>G
|
ENSP00000321345.5:p.Gln555Arg
|
|
ENST00000395227.2:c.458A>G
|
ENSP00000378652.2:p.Gln153Arg
|
|
ENST00000425614.3:c.899A>G
|
ENSP00000387640.2:p.Gln300Arg
|
|
ENST00000473881.2:c.*490A>G
|
ENSP00000486667.1:n.*490A>G
|
|
NM_144701.2:c.1664A>G
|
NP_653302.2:p.Gln555Arg
|
|
XM_005270516.2:c.902A>G
|
XP_005270573.1:p.Gln301Arg
|
|
XM_011540789.1:c.1754A>G
|
XP_011539091.1:p.Gln585Arg
|
|
XM_011540790.1:c.1664A>G
|
XP_011539092.1:p.Gln555Arg
|
|
XM_011540791.1:c.1664A>G
|
XP_011539093.1:p.Gln555Arg
|
|
XM_011540790.3:c.1664A>G
|
XP_011539092.1:p.Gln555Arg
|
|
XM_011540791.3:c.1664A>G
|
XP_011539093.1:p.Gln555Arg
|
|
XR_001736993.1:n.1744A>G
|
|
|
NM_144701.3:c.1664A>G
MANE Select
|
NP_653302.2:p.Gln555Arg
|
|