ENST00000697149.1:c.1446G>T
|
ENSP00000513138.1:n.1446G>T
|
|
ENST00000697150.1:c.1504G>T
|
ENSP00000513139.1:n.1504G>T
|
|
ENST00000697151.1:c.1437G>T
|
ENSP00000513140.1:n.1437G>T
|
|
ENST00000697164.1:c.1517G>T
|
ENSP00000513153.1:p.Ser506Ile
|
|
ENST00000697165.1:c.1304G>T
|
ENSP00000513154.1:p.Ser435Ile
|
|
ENST00000347310.10:c.1607G>T
MANE Select
|
ENSP00000321345.5:p.Ser536Ile
|
|
ENST00000637002.1:c.998G>T
|
ENSP00000490340.1:p.Ser333Ile
|
|
ENST00000347310.9:c.1607G>T
|
ENSP00000321345.5:p.Ser536Ile
|
|
ENST00000395227.2:c.401G>T
|
ENSP00000378652.2:p.Ser134Ile
|
|
ENST00000425614.3:c.842G>T
|
ENSP00000387640.2:p.Ser281Ile
|
|
ENST00000473881.2:c.*433G>T
|
ENSP00000486667.1:n.*433G>T
|
|
NM_144701.2:c.1607G>T
|
NP_653302.2:p.Ser536Ile
|
|
XM_005270516.2:c.845G>T
|
XP_005270573.1:p.Ser282Ile
|
|
XM_011540789.1:c.1697G>T
|
XP_011539091.1:p.Ser566Ile
|
|
XM_011540790.1:c.1607G>T
|
XP_011539092.1:p.Ser536Ile
|
|
XM_011540791.1:c.1607G>T
|
XP_011539093.1:p.Ser536Ile
|
|
XM_011540790.3:c.1607G>T
|
XP_011539092.1:p.Ser536Ile
|
|
XM_011540791.3:c.1607G>T
|
XP_011539093.1:p.Ser536Ile
|
|
XR_001736993.1:n.1687G>T
|
|
|
NM_144701.3:c.1607G>T
MANE Select
|
NP_653302.2:p.Ser536Ile
|
|