ENST00000689605.1:c.1923-3293G>A
(CLIP4)
|
ENSP00000508948.1:n.1923-3293G>A
|
|
ENST00000389048.8:c.4452C>T
(ALK)
MANE Select
|
ENSP00000373700.3:p.Asn1484=
|
|
ENST00000431873.6:c.1679C>T
(ALK)
|
|
|
ENST00000638605.1:n.1329C>T
(ALK)
|
|
|
ENST00000642122.1:c.1248C>T
(ALK)
|
ENSP00000493203.1:p.Asn416=
|
|
ENST00000389048.7:c.4452C>T
(ALK)
|
ENSP00000373700.3:p.Asn1484=
|
|
ENST00000431873.5:c.1332C>T
(ALK)
|
ENSP00000414027.2:p.Asn444=
|
|
ENST00000618119.4:c.3321C>T
(ALK)
|
ENSP00000482733.1:p.Asn1107=
|
|
NM_004304.4:c.4452C>T
(ALK)
|
NP_004295.2:p.Asn1484=
|
|
NM_001353765.1:c.1248C>T
(ALK)
|
NP_001340694.1:p.Asn416=
|
|
XM_024452778.1:c.1605C>T
(ALK)
|
XP_024308546.1:p.Asn535=
|
|
XM_024452779.1:c.1248C>T
(ALK)
|
XP_024308547.1:p.Asn416=
|
|
NM_004304.5:c.4452C>T
(ALK)
MANE Select
|
NP_004295.2:p.Asn1484=
|
|
NM_001353765.2:c.1248C>T
(ALK)
|
NP_001340694.1:p.Asn416=
|
|