ENST00000394867.9:n.1578C>T
|
|
|
ENST00000688002.1:n.3290C>T
|
|
|
ENST00000688751.1:n.275C>T
|
|
|
ENST00000689792.1:n.1043C>T
|
|
|
ENST00000262948.10:c.1139C>T
MANE Select
|
ENSP00000262948.4:p.Ala380Val
|
|
ENST00000262948.9:c.1139C>T
|
ENSP00000262948.3:p.Ala380Val
|
|
ENST00000394867.8:c.848C>T
|
ENSP00000378336.1:p.Ala283Val
|
|
ENST00000597263.5:n.324C>T
|
|
|
ENST00000599021.1:c.249C>T
|
|
|
ENST00000600584.5:n.2588C>T
|
|
|
ENST00000601786.5:n.1440C>T
|
|
|
NM_030662.3:c.1139C>T , LRG_750t1:c.1139C>T
|
NP_109587.1:p.Ala380Val
|
|
XM_006722799.2:c.860C>T
|
XP_006722862.1:p.Ala287Val
|
|
XM_011528133.1:c.569C>T
|
XP_011526435.1:p.Ala190Val
|
|
NM_030662.4:c.1139C>T
MANE Select
|
NP_109587.1:p.Ala380Val
|
|