ENST00000697149.1:c.1438T>C
|
ENSP00000513138.1:n.1438T>C
|
|
ENST00000697150.1:c.1496T>C
|
ENSP00000513139.1:n.1496T>C
|
|
ENST00000697151.1:c.1429T>C
|
ENSP00000513140.1:n.1429T>C
|
|
ENST00000697164.1:c.1509T>C
|
ENSP00000513153.1:p.Ser503=
|
|
ENST00000697165.1:c.1296T>C
|
ENSP00000513154.1:p.Ser432=
|
|
ENST00000347310.10:c.1599T>C
MANE Select
|
ENSP00000321345.5:p.Ser533=
|
|
ENST00000637002.1:c.990T>C
|
ENSP00000490340.1:p.Ser330=
|
|
ENST00000347310.9:c.1599T>C
|
ENSP00000321345.5:p.Ser533=
|
|
ENST00000395227.2:c.393T>C
|
ENSP00000378652.2:p.Ser131=
|
|
ENST00000425614.3:c.834T>C
|
ENSP00000387640.2:p.Ser278=
|
|
ENST00000473881.2:c.*425T>C
|
ENSP00000486667.1:n.*425T>C
|
|
NM_144701.2:c.1599T>C
|
NP_653302.2:p.Ser533=
|
|
XM_005270516.2:c.837T>C
|
XP_005270573.1:p.Ser279=
|
|
XM_011540789.1:c.1689T>C
|
XP_011539091.1:p.Ser563=
|
|
XM_011540790.1:c.1599T>C
|
XP_011539092.1:p.Ser533=
|
|
XM_011540791.1:c.1599T>C
|
XP_011539093.1:p.Ser533=
|
|
XM_011540790.3:c.1599T>C
|
XP_011539092.1:p.Ser533=
|
|
XM_011540791.3:c.1599T>C
|
XP_011539093.1:p.Ser533=
|
|
XR_001736993.1:n.1679T>C
|
|
|
NM_144701.3:c.1599T>C
MANE Select
|
NP_653302.2:p.Ser533=
|
|