|
ENST00000689605.1:c.*467G>A
(CLIP4)
|
ENSP00000508948.1:n.*467G>A
|
|
|
ENST00000389048.8:c.4073+69C>T
(ALK)
MANE Select
|
ENSP00000373700.3:n.4073+69C>T
|
|
|
ENST00000431873.6:c.1300+69C>T
(ALK)
|
|
|
|
ENST00000638605.1:n.950+69C>T
(ALK)
|
|
|
|
ENST00000642122.1:c.869+69C>T
(ALK)
|
ENSP00000493203.1:n.869+69C>T
|
|
|
ENST00000389048.7:c.4073+69C>T
(ALK)
|
ENSP00000373700.3:n.4073+69C>T
|
|
|
ENST00000431873.5:c.953+69C>T
(ALK)
|
ENSP00000414027.2:n.953+69C>T
|
|
|
ENST00000618119.4:c.2942+69C>T
(ALK)
|
ENSP00000482733.1:n.2942+69C>T
|
|
|
NM_004304.4:c.4073+69C>T
(ALK)
|
NP_004295.2:n.4073+69C>T
|
|
|
NM_001353765.1:c.869+69C>T
(ALK)
|
NP_001340694.1:n.869+69C>T
|
|
|
XM_024452778.1:c.1226+69C>T
(ALK)
|
XP_024308546.1:n.1226+69C>T
|
|
|
XM_024452779.1:c.869+69C>T
(ALK)
|
XP_024308547.1:n.869+69C>T
|
|
|
NM_004304.5:c.4073+69C>T
(ALK)
MANE Select
|
NP_004295.2:n.4073+69C>T
|
|
|
NM_001353765.2:c.869+69C>T
(ALK)
|
NP_001340694.1:n.869+69C>T
|
|
