ENST00000689605.1:c.*554T>A
(CLIP4)
|
ENSP00000508948.1:n.*554T>A
|
|
ENST00000389048.8:c.4055A>T
(ALK)
MANE Select
|
ENSP00000373700.3:p.Lys1352Met
|
|
ENST00000431873.6:c.1282A>T
(ALK)
|
|
|
ENST00000638605.1:n.932A>T
(ALK)
|
|
|
ENST00000642122.1:c.851A>T
(ALK)
|
ENSP00000493203.1:p.Lys284Met
|
|
ENST00000389048.7:c.4055A>T
(ALK)
|
ENSP00000373700.3:p.Lys1352Met
|
|
ENST00000431873.5:c.935A>T
(ALK)
|
ENSP00000414027.2:p.Lys312Met
|
|
ENST00000618119.4:c.2924A>T
(ALK)
|
ENSP00000482733.1:p.Lys975Met
|
|
NM_004304.4:c.4055A>T
(ALK)
|
NP_004295.2:p.Lys1352Met
|
|
NM_001353765.1:c.851A>T
(ALK)
|
NP_001340694.1:p.Lys284Met
|
|
XM_024452778.1:c.1208A>T
(ALK)
|
XP_024308546.1:p.Lys403Met
|
|
XM_024452779.1:c.851A>T
(ALK)
|
XP_024308547.1:p.Lys284Met
|
|
NM_004304.5:c.4055A>T
(ALK)
MANE Select
|
NP_004295.2:p.Lys1352Met
|
|
NM_001353765.2:c.851A>T
(ALK)
|
NP_001340694.1:p.Lys284Met
|
|