|
ENST00000689605.1:c.1923-3222_1923-3221delinsCT
(CLIP4)
|
ENSP00000508948.1:n.1923-3222_1923-3221delinsCT
|
|
|
ENST00000389048.8:c.4380_4381delinsAG
(ALK)
MANE Select
|
ENSP00000373700.3:p.Ile1461Val
|
|
|
ENST00000431873.6:c.1607_1608delinsAG
(ALK)
|
|
|
|
ENST00000638605.1:n.1257_1258delinsAG
(ALK)
|
|
|
|
ENST00000642122.1:c.1176_1177delinsAG
(ALK)
|
ENSP00000493203.1:p.Ile393Val
|
|
|
ENST00000389048.7:c.4380_4381delinsAG
(ALK)
|
ENSP00000373700.3:p.Ile1461Val
|
|
|
ENST00000431873.5:c.1260_1261delinsAG
(ALK)
|
ENSP00000414027.2:p.Ile421Val
|
|
|
ENST00000618119.4:c.3249_3250delinsAG
(ALK)
|
ENSP00000482733.1:p.Ile1084Val
|
|
|
NM_004304.4:c.4380_4381delinsAG
(ALK)
|
NP_004295.2:p.Ile1461Val
|
|
|
NM_001353765.1:c.1176_1177delinsAG
(ALK)
|
NP_001340694.1:p.Ile393Val
|
|
|
XM_024452778.1:c.1533_1534delinsAG
(ALK)
|
XP_024308546.1:p.Ile512Val
|
|
|
XM_024452779.1:c.1176_1177delinsAG
(ALK)
|
XP_024308547.1:p.Ile393Val
|
|
|
NM_004304.5:c.4380_4381delinsAG
(ALK)
MANE Select
|
NP_004295.2:p.Ile1461Val
|
|
|
NM_001353765.2:c.1176_1177delinsAG
(ALK)
|
NP_001340694.1:p.Ile393Val
|
|
