ENST00000219548.9:c.415C>G
(STUB1)
MANE Select
|
ENSP00000219548.4:p.Leu139Val
|
|
ENST00000219548.8:c.415C>G
(STUB1)
|
ENSP00000219548.4:p.Leu139Val
|
|
ENST00000563505.5:n.511C>G
(STUB1)
|
|
|
ENST00000564316.1:c.14C>G
(STUB1)
|
|
|
ENST00000564370.5:c.199C>G
(STUB1)
|
ENSP00000456875.1:p.Leu67Val
|
|
ENST00000565677.5:c.199C>G
(STUB1)
|
ENSP00000457228.1:p.Leu67Val
|
|
ENST00000566181.2:n.184C>G
(STUB1)
|
|
|
ENST00000566408.5:c.132C>G
(STUB1)
|
|
|
ENST00000567173.5:c.358C>G
(STUB1)
|
ENSP00000456591.1:p.Leu120Val
|
|
ENST00000569248.5:n.989C>G
(STUB1)
|
|
|
ENST00000620831.4:c.-50+38191C>G
(MSLN)
|
ENSP00000482893.1:n.-50+38191C>G
|
|
NM_001293197.1:c.199C>G
(STUB1)
|
NP_001280126.1:p.Leu67Val
|
|
NM_005861.3:c.415C>G
(STUB1)
|
NP_005852.2:p.Leu139Val
|
|
NM_005861.4:c.415C>G
(STUB1)
MANE Select
|
NP_005852.2:p.Leu139Val
|
|
NM_001293197.2:c.199C>G
(STUB1)
|
NP_001280126.1:p.Leu67Val
|
|