|
ENST00000689605.1:c.*758C>A
(CLIP4)
|
ENSP00000508948.1:n.*758C>A
|
|
|
ENST00000389048.8:c.3939-88G>T
(ALK)
MANE Select
|
ENSP00000373700.3:n.3939-88G>T
|
|
|
ENST00000431873.6:c.1166-88G>T
(ALK)
|
|
|
|
ENST00000638605.1:n.816-88G>T
(ALK)
|
|
|
|
ENST00000642122.1:c.735-88G>T
(ALK)
|
ENSP00000493203.1:n.735-88G>T
|
|
|
ENST00000389048.7:c.3939-88G>T
(ALK)
|
ENSP00000373700.3:n.3939-88G>T
|
|
|
ENST00000431873.5:c.819-88G>T
(ALK)
|
ENSP00000414027.2:n.819-88G>T
|
|
|
ENST00000618119.4:c.2808-88G>T
(ALK)
|
ENSP00000482733.1:n.2808-88G>T
|
|
|
NM_004304.4:c.3939-88G>T
(ALK)
|
NP_004295.2:n.3939-88G>T
|
|
|
NM_001353765.1:c.735-88G>T
(ALK)
|
NP_001340694.1:n.735-88G>T
|
|
|
XM_024452778.1:c.1092-88G>T
(ALK)
|
XP_024308546.1:n.1092-88G>T
|
|
|
XM_024452779.1:c.735-88G>T
(ALK)
|
XP_024308547.1:n.735-88G>T
|
|
|
NM_004304.5:c.3939-88G>T
(ALK)
MANE Select
|
NP_004295.2:n.3939-88G>T
|
|
|
NM_001353765.2:c.735-88G>T
(ALK)
|
NP_001340694.1:n.735-88G>T
|
|
