ENST00000689605.1:c.*582T>C
(CLIP4)
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ENSP00000508948.1:n.*582T>C
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ENST00000389048.8:c.4027A>G
(ALK)
MANE Select
|
ENSP00000373700.3:p.Thr1343Ala
|
|
ENST00000431873.6:c.1254A>G
(ALK)
|
|
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ENST00000638605.1:n.904A>G
(ALK)
|
|
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ENST00000642122.1:c.823A>G
(ALK)
|
ENSP00000493203.1:p.Thr275Ala
|
|
ENST00000389048.7:c.4027A>G
(ALK)
|
ENSP00000373700.3:p.Thr1343Ala
|
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ENST00000431873.5:c.907A>G
(ALK)
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ENSP00000414027.2:p.Thr303Ala
|
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ENST00000618119.4:c.2896A>G
(ALK)
|
ENSP00000482733.1:p.Thr966Ala
|
|
NM_004304.4:c.4027A>G
(ALK)
|
NP_004295.2:p.Thr1343Ala
|
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NM_001353765.1:c.823A>G
(ALK)
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NP_001340694.1:p.Thr275Ala
|
|
XM_024452778.1:c.1180A>G
(ALK)
|
XP_024308546.1:p.Thr394Ala
|
|
XM_024452779.1:c.823A>G
(ALK)
|
XP_024308547.1:p.Thr275Ala
|
|
NM_004304.5:c.4027A>G
(ALK)
MANE Select
|
NP_004295.2:p.Thr1343Ala
|
|
NM_001353765.2:c.823A>G
(ALK)
|
NP_001340694.1:p.Thr275Ala
|
|