ENST00000431168.2:c.269C>T
|
ENSP00000393455.2:p.Ala90Val
|
|
ENST00000292327.6:c.269C>T
MANE Select
|
ENSP00000292327.4:p.Ala90Val
|
|
ENST00000653454.1:c.269C>T
|
ENSP00000499624.1:p.Ala90Val
|
|
ENST00000654597.1:c.269C>T
|
ENSP00000499406.1:p.Ala90Val
|
|
ENST00000655244.1:n.491C>T
|
|
|
ENST00000662933.1:c.269C>T
|
ENSP00000499577.1:p.Ala90Val
|
|
ENST00000664891.1:n.227C>T
|
|
|
ENST00000292327.4:c.269C>T
|
ENSP00000292327.4:p.Ala90Val
|
|
ENST00000395869.5:c.269C>T
|
ENSP00000379210.1:p.Ala90Val
|
|
NM_000258.2:c.269C>T , LRG_395t1:c.269C>T
|
NP_000249.1:p.Ala90Val
|
|
NM_000258.3:c.269C>T
MANE Select
|
NP_000249.1:p.Ala90Val
|
|