ENST00000326003.7:c.732C>T
MANE Select
|
ENSP00000314151.1:p.Thr244=
|
|
ENST00000326003.6:c.732C>T
|
ENSP00000314151.1:p.Thr244=
|
|
ENST00000360617.7:c.1174C>T
|
ENSP00000353829.2:n.1174C>T
|
|
ENST00000422986.6:c.*388C>T
|
ENSP00000393628.2:n.*388C>T
|
|
ENST00000595392.5:c.*233C>T
|
ENSP00000468912.1:n.*233C>T
|
|
ENST00000595952.5:c.603C>T
|
ENSP00000471155.1:p.Thr201=
|
|
ENST00000596333.1:n.910C>T
|
|
|
ENST00000598145.1:c.734C>T
|
|
|
ENST00000601349.5:n.2011C>T
|
|
|
ENST00000601812.1:n.1164C>T
|
|
|
ENST00000617027.4:c.609C>T
|
ENSP00000483513.1:p.Thr203=
|
|
NM_001030047.1:c.*457C>T
|
NP_001025218.1:n.*457C>T
|
|
NM_001030048.1:c.603C>T
|
NP_001025219.1:p.Thr201=
|
|
NM_001648.2:c.732C>T
MANE Select
|
NP_001639.1:p.Thr244=
|
|
XM_011526923.1:c.750C>T
|
XP_011525225.1:p.Thr250=
|
|
XR_935817.1:n.1324+819C>T
|
|
|