|
NM_004304.5:c.4607A>G
(ALK)
MANE Select
|
NP_004295.2:p.Glu1536Gly
|
|
ENST00000389048.8:c.4607A>G
(ALK)
MANE Select
|
ENSP00000373700.3:p.Glu1536Gly
|
|
NM_001353765.1:c.1403A>G
(ALK)
|
NP_001340694.1:p.Glu468Gly
|
|
NM_001353765.2:c.1403A>G
(ALK)
|
NP_001340694.1:p.Glu468Gly
|
|
NM_004304.4:c.4607A>G
(ALK)
|
NP_004295.2:p.Glu1536Gly
|
|
ENST00000389048.7:c.4607A>G
(ALK)
|
ENSP00000373700.3:p.Glu1536Gly
|
|
ENST00000431873.5:c.1487A>G
(ALK)
|
ENSP00000414027.2:p.Glu496Gly
|
|
ENST00000431873.6:c.1834A>G
(ALK)
|
|
|
ENST00000618119.4:c.3476A>G
(ALK)
|
ENSP00000482733.1:p.Glu1159Gly
|
|
ENST00000638605.1:n.1484A>G
(ALK)
|
|
|
ENST00000642122.1:c.1403A>G
(ALK)
|
ENSP00000493203.1:p.Glu468Gly
|
|
ENST00000689605.1:c.1923-3448T>C
(CLIP4)
|
ENSP00000508948.1:n.1923-3448T>C
|
|
XM_024452778.1:c.1760A>G
(ALK)
|
XP_024308546.1:p.Glu587Gly
|
|
XM_024452779.1:c.1403A>G
(ALK)
|
XP_024308547.1:p.Glu468Gly
|