|
ENST00000689605.1:c.1923-3648G>A
(CLIP4)
|
ENSP00000508948.1:n.1923-3648G>A
|
|
|
ENST00000389048.8:c.4807C>T
(ALK)
MANE Select
|
ENSP00000373700.3:p.His1603Tyr
|
|
|
ENST00000431873.6:c.2034C>T
(ALK)
|
|
|
|
ENST00000638605.1:n.1684C>T
(ALK)
|
|
|
|
ENST00000642122.1:c.1603C>T
(ALK)
|
ENSP00000493203.1:p.His535Tyr
|
|
|
ENST00000389048.7:c.4807C>T
(ALK)
|
ENSP00000373700.3:p.His1603Tyr
|
|
|
ENST00000431873.5:c.1687C>T
(ALK)
|
ENSP00000414027.2:p.His563Tyr
|
|
|
ENST00000618119.4:c.3676C>T
(ALK)
|
ENSP00000482733.1:p.His1226Tyr
|
|
|
NM_004304.4:c.4807C>T
(ALK)
|
NP_004295.2:p.His1603Tyr
|
|
|
NM_001353765.1:c.1603C>T
(ALK)
|
NP_001340694.1:p.His535Tyr
|
|
|
XM_024452778.1:c.1960C>T
(ALK)
|
XP_024308546.1:p.His654Tyr
|
|
|
XM_024452779.1:c.1603C>T
(ALK)
|
XP_024308547.1:p.His535Tyr
|
|
|
NM_004304.5:c.4807C>T
(ALK)
MANE Select
|
NP_004295.2:p.His1603Tyr
|
|
|
NM_001353765.2:c.1603C>T
(ALK)
|
NP_001340694.1:p.His535Tyr
|
|
