ENST00000326003.7:c.722C>A
MANE Select
|
ENSP00000314151.1:p.Ser241Tyr
|
|
ENST00000326003.6:c.722C>A
|
ENSP00000314151.1:p.Ser241Tyr
|
|
ENST00000360617.7:c.1164C>A
|
ENSP00000353829.2:n.1164C>A
|
|
ENST00000422986.6:c.*378C>A
|
ENSP00000393628.2:n.*378C>A
|
|
ENST00000595392.5:c.*223C>A
|
ENSP00000468912.1:n.*223C>A
|
|
ENST00000595952.5:c.593C>A
|
ENSP00000471155.1:p.Ser198Tyr
|
|
ENST00000596333.1:n.900C>A
|
|
|
ENST00000598145.1:c.724C>A
|
|
|
ENST00000601349.5:n.2001C>A
|
|
|
ENST00000601812.1:n.1154C>A
|
|
|
ENST00000617027.4:c.599C>A
|
ENSP00000483513.1:p.Ser200Tyr
|
|
NM_001030047.1:c.*447C>A
|
NP_001025218.1:n.*447C>A
|
|
NM_001030048.1:c.593C>A
|
NP_001025219.1:p.Ser198Tyr
|
|
NM_001648.2:c.722C>A
MANE Select
|
NP_001639.1:p.Ser241Tyr
|
|
XM_011526923.1:c.740C>A
|
XP_011525225.1:p.Ser247Tyr
|
|
XR_935817.1:n.1324+809C>A
|
|
|