ENST00000222572.8:c.-9T>A
MANE Select
|
ENSP00000222572.3:n.-9T>A
|
|
ENST00000222572.7:c.-9T>A
|
ENSP00000222572.3:n.-9T>A
|
|
ENST00000433091.6:c.-9T>A
|
ENSP00000404622.2:n.-9T>A
|
|
ENST00000446142.5:c.-9T>A
|
ENSP00000405211.1:n.-9T>A
|
|
ENST00000455123.5:c.-9T>A
|
ENSP00000414515.1:n.-9T>A
|
|
ENST00000469716.1:n.69T>A
|
|
|
ENST00000469926.5:c.-266T>A
|
ENSP00000488550.1:n.-266T>A
|
|
ENST00000471883.1:n.71T>A
|
|
|
ENST00000490778.5:c.-321T>A
|
ENSP00000488826.1:n.-321T>A
|
|
ENST00000493290.5:c.-342T>A
|
ENSP00000488822.1:n.-342T>A
|
|
ENST00000493469.5:n.4T>A
|
|
|
ENST00000632034.1:c.-9T>A
|
ENSP00000487898.1:n.-9T>A
|
|
ENST00000633192.1:c.55T>A
|
ENSP00000488378.1:p.Ser19Thr
|
|
ENST00000633531.1:c.-9T>A
|
ENSP00000488838.1:n.-9T>A
|
|
NM_000305.2:c.-9T>A
|
NP_000296.2:n.-9T>A
|
|
NM_001018161.1:c.-9T>A
|
NP_001018171.1:n.-9T>A
|
|
XM_005250453.1:c.-187T>A
|
XP_005250510.1:n.-187T>A
|
|
XM_005250454.1:c.-263T>A
|
XP_005250511.1:n.-263T>A
|
|
XM_011516333.1:c.-337T>A
|
XP_011514635.1:n.-337T>A
|
|
XM_017012357.2:c.-263T>A
|
XP_016867846.1:n.-263T>A
|
|
XM_017012358.2:c.-337T>A
|
XP_016867847.1:n.-337T>A
|
|
NM_000305.3:c.-9T>A
MANE Select
|
NP_000296.2:n.-9T>A
|
|
NM_001018161.2:c.-9T>A
|
NP_001018171.1:n.-9T>A
|
|