ENST00000689605.1:c.*206_*207insAATTGGAA
(CLIP4)
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ENSP00000508948.1:n.*206_*207insAATTGGAA
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ENST00000389048.8:c.4073+329_4073+330insTTCCAATT
(ALK)
MANE Select
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ENSP00000373700.3:n.4073+329_4073+330insTTCCAATT
|
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ENST00000431873.6:c.1300+329_1300+330insTTCCAATT
(ALK)
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|
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ENST00000638605.1:n.950+329_950+330insTTCCAATT
(ALK)
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ENST00000642122.1:c.869+329_869+330insTTCCAATT
(ALK)
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ENSP00000493203.1:n.869+329_869+330insTTCCAATT
|
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ENST00000389048.7:c.4073+329_4073+330insTTCCAATT
(ALK)
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ENSP00000373700.3:n.4073+329_4073+330insTTCCAATT
|
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ENST00000431873.5:c.953+329_953+330insTTCCAATT
(ALK)
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ENSP00000414027.2:n.953+329_953+330insTTCCAATT
|
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ENST00000618119.4:c.2942+329_2942+330insTTCCAATT
(ALK)
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ENSP00000482733.1:n.2942+329_2942+330insTTCCAATT
|
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NM_004304.4:c.4073+329_4073+330insTTCCAATT
(ALK)
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NP_004295.2:n.4073+329_4073+330insTTCCAATT
|
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NM_001353765.1:c.869+329_869+330insTTCCAATT
(ALK)
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NP_001340694.1:n.869+329_869+330insTTCCAATT
|
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XM_024452778.1:c.1226+329_1226+330insTTCCAATT
(ALK)
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XP_024308546.1:n.1226+329_1226+330insTTCCAATT
|
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XM_024452779.1:c.869+329_869+330insTTCCAATT
(ALK)
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XP_024308547.1:n.869+329_869+330insTTCCAATT
|
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NM_004304.5:c.4073+329_4073+330insTTCCAATT
(ALK)
MANE Select
|
NP_004295.2:n.4073+329_4073+330insTTCCAATT
|
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NM_001353765.2:c.869+329_869+330insTTCCAATT
(ALK)
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NP_001340694.1:n.869+329_869+330insTTCCAATT
|
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