ENST00000697149.1:c.1540A>G
|
ENSP00000513138.1:n.1540A>G
|
|
ENST00000697150.1:c.1598A>G
|
ENSP00000513139.1:n.1598A>G
|
|
ENST00000697151.1:c.1531A>G
|
ENSP00000513140.1:n.1531A>G
|
|
ENST00000697164.1:c.1611A>G
|
ENSP00000513153.1:p.Val537=
|
|
ENST00000697165.1:c.1398A>G
|
ENSP00000513154.1:p.Val466=
|
|
ENST00000347310.10:c.1701A>G
MANE Select
|
ENSP00000321345.5:p.Val567=
|
|
ENST00000637002.1:c.1092A>G
|
ENSP00000490340.1:p.Val364=
|
|
ENST00000347310.9:c.1701A>G
|
ENSP00000321345.5:p.Val567=
|
|
ENST00000395227.2:c.495A>G
|
ENSP00000378652.2:p.Val165=
|
|
ENST00000425614.3:c.936A>G
|
ENSP00000387640.2:p.Val312=
|
|
ENST00000473881.2:c.*527A>G
|
ENSP00000486667.1:n.*527A>G
|
|
NM_144701.2:c.1701A>G
|
NP_653302.2:p.Val567=
|
|
XM_005270516.2:c.939A>G
|
XP_005270573.1:p.Val313=
|
|
XM_011540789.1:c.1791A>G
|
XP_011539091.1:p.Val597=
|
|
XM_011540790.1:c.1701A>G
|
XP_011539092.1:p.Val567=
|
|
XM_011540791.1:c.1701A>G
|
XP_011539093.1:p.Val567=
|
|
XM_011540790.3:c.1701A>G
|
XP_011539092.1:p.Val567=
|
|
XM_011540791.3:c.1701A>G
|
XP_011539093.1:p.Val567=
|
|
XR_001736993.1:n.1781A>G
|
|
|
NM_144701.3:c.1701A>G
MANE Select
|
NP_653302.2:p.Val567=
|
|