ENST00000326003.7:c.767C=
MANE Select
|
ENSP00000314151.1:p.Thr256=
|
|
ENST00000326003.6:c.767C=
|
ENSP00000314151.1:p.Thr256=
|
|
ENST00000360617.7:c.1209C=
|
ENSP00000353829.2:n.1209C=
|
|
ENST00000422986.6:c.*423C=
|
ENSP00000393628.2:n.*423C=
|
|
ENST00000595392.5:c.*268C=
|
ENSP00000468912.1:n.*268C=
|
|
ENST00000595952.5:c.638C=
|
ENSP00000471155.1:p.Thr213=
|
|
ENST00000596333.1:n.945C=
|
|
|
ENST00000598145.1:c.769C=
|
|
|
ENST00000601349.5:n.2046C=
|
|
|
ENST00000601812.1:n.1199C=
|
|
|
ENST00000617027.4:c.644C=
|
ENSP00000483513.1:p.Thr215=
|
|
NM_001030047.1:c.*492C=
|
NP_001025218.1:n.*492C=
|
|
NM_001030048.1:c.638C=
|
NP_001025219.1:p.Thr213=
|
|
NM_001648.2:c.767C=
MANE Select
|
NP_001639.1:p.Thr256=
|
|
XM_011526923.1:c.785C=
|
XP_011525225.1:p.Thr262=
|
|
XR_935817.1:n.1324+854C=
|
|
|