ENST00000394867.9:n.1635C>T
|
|
|
ENST00000688002.1:n.3347C>T
|
|
|
ENST00000688751.1:n.332C>T
|
|
|
ENST00000689792.1:n.1100C>T
|
|
|
ENST00000262948.10:c.1196C>T
MANE Select
|
ENSP00000262948.4:p.Ala399Val
|
|
ENST00000262948.9:c.1196C>T
|
ENSP00000262948.3:p.Ala399Val
|
|
ENST00000394867.8:c.905C>T
|
ENSP00000378336.1:p.Ala302Val
|
|
ENST00000597263.5:n.381C>T
|
|
|
ENST00000599021.1:c.306C>T
|
|
|
ENST00000600584.5:n.2645C>T
|
|
|
ENST00000601786.5:n.1497C>T
|
|
|
NM_030662.3:c.1196C>T , LRG_750t1:c.1196C>T
|
NP_109587.1:p.Ala399Val
|
|
XM_006722799.2:c.917C>T
|
XP_006722862.1:p.Ala306Val
|
|
XM_011528133.1:c.626C>T
|
XP_011526435.1:p.Ala209Val
|
|
NM_030662.4:c.1196C>T
MANE Select
|
NP_109587.1:p.Ala399Val
|
|