|
NM_004304.5:c.4340C>T
(ALK)
MANE Select
|
NP_004295.2:p.Thr1447Ile
|
|
ENST00000389048.8:c.4340C>T
(ALK)
MANE Select
|
ENSP00000373700.3:p.Thr1447Ile
|
|
NM_001353765.1:c.1136C>T
(ALK)
|
NP_001340694.1:p.Thr379Ile
|
|
NM_001353765.2:c.1136C>T
(ALK)
|
NP_001340694.1:p.Thr379Ile
|
|
NM_004304.4:c.4340C>T
(ALK)
|
NP_004295.2:p.Thr1447Ile
|
|
ENST00000389048.7:c.4340C>T
(ALK)
|
ENSP00000373700.3:p.Thr1447Ile
|
|
ENST00000431873.5:c.1220C>T
(ALK)
|
ENSP00000414027.2:p.Thr407Ile
|
|
ENST00000431873.6:c.1567C>T
(ALK)
|
|
|
ENST00000618119.4:c.3209C>T
(ALK)
|
ENSP00000482733.1:p.Thr1070Ile
|
|
ENST00000638605.1:n.1217C>T
(ALK)
|
|
|
ENST00000642122.1:c.1136C>T
(ALK)
|
ENSP00000493203.1:p.Thr379Ile
|
|
ENST00000689605.1:c.1923-3181G>A
(CLIP4)
|
ENSP00000508948.1:n.1923-3181G>A
|
|
XM_024452778.1:c.1493C>T
(ALK)
|
XP_024308546.1:p.Thr498Ile
|
|
XM_024452779.1:c.1136C>T
(ALK)
|
XP_024308547.1:p.Thr379Ile
|
