ENST00000326003.7:c.763G>T
MANE Select
|
ENSP00000314151.1:p.Asp255Tyr
|
|
ENST00000326003.6:c.763G>T
|
ENSP00000314151.1:p.Asp255Tyr
|
|
ENST00000360617.7:c.1205G>T
|
ENSP00000353829.2:n.1205G>T
|
|
ENST00000422986.6:c.*419G>T
|
ENSP00000393628.2:n.*419G>T
|
|
ENST00000595392.5:c.*264G>T
|
ENSP00000468912.1:n.*264G>T
|
|
ENST00000595952.5:c.634G>T
|
ENSP00000471155.1:p.Asp212Tyr
|
|
ENST00000596333.1:n.941G>T
|
|
|
ENST00000598145.1:c.765G>T
|
|
|
ENST00000601349.5:n.2042G>T
|
|
|
ENST00000601812.1:n.1195G>T
|
|
|
ENST00000617027.4:c.640G>T
|
ENSP00000483513.1:p.Asp214Tyr
|
|
NM_001030047.1:c.*488G>T
|
NP_001025218.1:n.*488G>T
|
|
NM_001030048.1:c.634G>T
|
NP_001025219.1:p.Asp212Tyr
|
|
NM_001648.2:c.763G>T
MANE Select
|
NP_001639.1:p.Asp255Tyr
|
|
XM_011526923.1:c.781G>T
|
XP_011525225.1:p.Asp261Tyr
|
|
XR_935817.1:n.1324+850G>T
|
|
|