ENST00000326003.7:c.631-159G>T
MANE Select
|
ENSP00000314151.1:n.631-159G>T
|
|
ENST00000326003.6:c.631-159G>T
|
ENSP00000314151.1:n.631-159G>T
|
|
ENST00000360617.7:c.914G>T
|
ENSP00000353829.2:n.914G>T
|
|
ENST00000422986.6:c.*287-159G>T
|
ENSP00000393628.2:n.*287-159G>T
|
|
ENST00000595392.5:c.*132-159G>T
|
ENSP00000468912.1:n.*132-159G>T
|
|
ENST00000595952.5:c.502-159G>T
|
ENSP00000471155.1:n.502-159G>T
|
|
ENST00000596185.5:c.*739-159G>T
|
ENSP00000471648.1:n.*739-159G>T
|
|
ENST00000596333.1:n.809-159G>T
|
|
|
ENST00000598145.1:c.633-159G>T
|
|
|
ENST00000601349.5:n.1910-159G>T
|
|
|
ENST00000601812.1:n.1063-159G>T
|
|
|
ENST00000617027.4:c.508-159G>T
|
ENSP00000483513.1:n.508-159G>T
|
|
NM_001030047.1:c.*197G>T
|
NP_001025218.1:n.*197G>T
|
|
NM_001030048.1:c.502-159G>T
|
NP_001025219.1:n.502-159G>T
|
|
NM_001648.2:c.631-159G>T
MANE Select
|
NP_001639.1:n.631-159G>T
|
|
XM_011526923.1:c.649-159G>T
|
XP_011525225.1:n.649-159G>T
|
|
XM_011526924.1:c.*197G>T
|
XP_011525226.1:n.*197G>T
|
|
XR_935817.1:n.1324+559G>T
|
|
|