ENST00000689605.1:c.*577A>T
(CLIP4)
|
ENSP00000508948.1:n.*577A>T
|
|
ENST00000389048.8:c.4032T>A
(ALK)
MANE Select
|
ENSP00000373700.3:p.Ser1344Arg
|
|
ENST00000431873.6:c.1259T>A
(ALK)
|
|
|
ENST00000638605.1:n.909T>A
(ALK)
|
|
|
ENST00000642122.1:c.828T>A
(ALK)
|
ENSP00000493203.1:p.Ser276Arg
|
|
ENST00000389048.7:c.4032T>A
(ALK)
|
ENSP00000373700.3:p.Ser1344Arg
|
|
ENST00000431873.5:c.912T>A
(ALK)
|
ENSP00000414027.2:p.Ser304Arg
|
|
ENST00000618119.4:c.2901T>A
(ALK)
|
ENSP00000482733.1:p.Ser967Arg
|
|
NM_004304.4:c.4032T>A
(ALK)
|
NP_004295.2:p.Ser1344Arg
|
|
NM_001353765.1:c.828T>A
(ALK)
|
NP_001340694.1:p.Ser276Arg
|
|
XM_024452778.1:c.1185T>A
(ALK)
|
XP_024308546.1:p.Ser395Arg
|
|
XM_024452779.1:c.828T>A
(ALK)
|
XP_024308547.1:p.Ser276Arg
|
|
NM_004304.5:c.4032T>A
(ALK)
MANE Select
|
NP_004295.2:p.Ser1344Arg
|
|
NM_001353765.2:c.828T>A
(ALK)
|
NP_001340694.1:p.Ser276Arg
|
|