ENST00000697149.1:c.1528A>C
|
ENSP00000513138.1:n.1528A>C
|
|
ENST00000697150.1:c.1586A>C
|
ENSP00000513139.1:n.1586A>C
|
|
ENST00000697151.1:c.1519A>C
|
ENSP00000513140.1:n.1519A>C
|
|
ENST00000697164.1:c.1599A>C
|
ENSP00000513153.1:p.Ile533=
|
|
ENST00000697165.1:c.1386A>C
|
ENSP00000513154.1:p.Ile462=
|
|
ENST00000347310.10:c.1689A>C
MANE Select
|
ENSP00000321345.5:p.Ile563=
|
|
ENST00000637002.1:c.1080A>C
|
ENSP00000490340.1:p.Ile360=
|
|
ENST00000347310.9:c.1689A>C
|
ENSP00000321345.5:p.Ile563=
|
|
ENST00000395227.2:c.483A>C
|
ENSP00000378652.2:p.Ile161=
|
|
ENST00000425614.3:c.924A>C
|
ENSP00000387640.2:p.Ile308=
|
|
ENST00000473881.2:c.*515A>C
|
ENSP00000486667.1:n.*515A>C
|
|
NM_144701.2:c.1689A>C
|
NP_653302.2:p.Ile563=
|
|
XM_005270516.2:c.927A>C
|
XP_005270573.1:p.Ile309=
|
|
XM_011540789.1:c.1779A>C
|
XP_011539091.1:p.Ile593=
|
|
XM_011540790.1:c.1689A>C
|
XP_011539092.1:p.Ile563=
|
|
XM_011540791.1:c.1689A>C
|
XP_011539093.1:p.Ile563=
|
|
XM_011540790.3:c.1689A>C
|
XP_011539092.1:p.Ile563=
|
|
XM_011540791.3:c.1689A>C
|
XP_011539093.1:p.Ile563=
|
|
XR_001736993.1:n.1769A>C
|
|
|
NM_144701.3:c.1689A>C
MANE Select
|
NP_653302.2:p.Ile563=
|
|