ENST00000689605.1:c.*541C>G
(CLIP4)
|
ENSP00000508948.1:n.*541C>G
|
|
ENST00000389048.8:c.4068G>C
(ALK)
MANE Select
|
ENSP00000373700.3:p.Gly1356=
|
|
ENST00000431873.6:c.1295G>C
(ALK)
|
|
|
ENST00000638605.1:n.945G>C
(ALK)
|
|
|
ENST00000642122.1:c.864G>C
(ALK)
|
ENSP00000493203.1:p.Gly288=
|
|
ENST00000389048.7:c.4068G>C
(ALK)
|
ENSP00000373700.3:p.Gly1356=
|
|
ENST00000431873.5:c.948G>C
(ALK)
|
ENSP00000414027.2:p.Gly316=
|
|
ENST00000618119.4:c.2937G>C
(ALK)
|
ENSP00000482733.1:p.Gly979=
|
|
NM_004304.4:c.4068G>C
(ALK)
|
NP_004295.2:p.Gly1356=
|
|
NM_001353765.1:c.864G>C
(ALK)
|
NP_001340694.1:p.Gly288=
|
|
XM_024452778.1:c.1221G>C
(ALK)
|
XP_024308546.1:p.Gly407=
|
|
XM_024452779.1:c.864G>C
(ALK)
|
XP_024308547.1:p.Gly288=
|
|
NM_004304.5:c.4068G>C
(ALK)
MANE Select
|
NP_004295.2:p.Gly1356=
|
|
NM_001353765.2:c.864G>C
(ALK)
|
NP_001340694.1:p.Gly288=
|
|