ENST00000219548.9:c.413C>T
(STUB1)
MANE Select
|
ENSP00000219548.4:p.Ala138Val
|
|
ENST00000219548.8:c.413C>T
(STUB1)
|
ENSP00000219548.4:p.Ala138Val
|
|
ENST00000563505.5:n.509C>T
(STUB1)
|
|
|
ENST00000564316.1:c.12C>T
(STUB1)
|
|
|
ENST00000564370.5:c.197C>T
(STUB1)
|
ENSP00000456875.1:p.Ala66Val
|
|
ENST00000565677.5:c.197C>T
(STUB1)
|
ENSP00000457228.1:p.Ala66Val
|
|
ENST00000566181.2:n.182C>T
(STUB1)
|
|
|
ENST00000566408.5:c.130C>T
(STUB1)
|
|
|
ENST00000567173.5:c.356C>T
(STUB1)
|
ENSP00000456591.1:p.Ala119Val
|
|
ENST00000569248.5:n.987C>T
(STUB1)
|
|
|
ENST00000620831.4:c.-50+38189C>T
(MSLN)
|
ENSP00000482893.1:n.-50+38189C>T
|
|
NM_001293197.1:c.197C>T
(STUB1)
|
NP_001280126.1:p.Ala66Val
|
|
NM_005861.3:c.413C>T
(STUB1)
|
NP_005852.2:p.Ala138Val
|
|
NM_005861.4:c.413C>T
(STUB1)
MANE Select
|
NP_005852.2:p.Ala138Val
|
|
NM_001293197.2:c.197C>T
(STUB1)
|
NP_001280126.1:p.Ala66Val
|
|