ENST00000689605.1:c.1923-3202T>C
(CLIP4)
|
ENSP00000508948.1:n.1923-3202T>C
|
|
ENST00000389048.8:c.4361A>G
(ALK)
MANE Select
|
ENSP00000373700.3:p.Lys1454Arg
|
|
ENST00000431873.6:c.1588A>G
(ALK)
|
|
|
ENST00000638605.1:n.1238A>G
(ALK)
|
|
|
ENST00000642122.1:c.1157A>G
(ALK)
|
ENSP00000493203.1:p.Lys386Arg
|
|
ENST00000389048.7:c.4361A>G
(ALK)
|
ENSP00000373700.3:p.Lys1454Arg
|
|
ENST00000431873.5:c.1241A>G
(ALK)
|
ENSP00000414027.2:p.Lys414Arg
|
|
ENST00000618119.4:c.3230A>G
(ALK)
|
ENSP00000482733.1:p.Lys1077Arg
|
|
NM_004304.4:c.4361A>G
(ALK)
|
NP_004295.2:p.Lys1454Arg
|
|
NM_001353765.1:c.1157A>G
(ALK)
|
NP_001340694.1:p.Lys386Arg
|
|
XM_024452778.1:c.1514A>G
(ALK)
|
XP_024308546.1:p.Lys505Arg
|
|
XM_024452779.1:c.1157A>G
(ALK)
|
XP_024308547.1:p.Lys386Arg
|
|
NM_004304.5:c.4361A>G
(ALK)
MANE Select
|
NP_004295.2:p.Lys1454Arg
|
|
NM_001353765.2:c.1157A>G
(ALK)
|
NP_001340694.1:p.Lys386Arg
|
|