ENST00000394867.9:n.1612G=
|
|
|
ENST00000688002.1:n.3324G=
|
|
|
ENST00000688751.1:n.309G=
|
|
|
ENST00000689792.1:n.1077G=
|
|
|
ENST00000262948.10:c.1173G=
MANE Select
|
ENSP00000262948.4:p.Gln391=
|
|
ENST00000262948.9:c.1173G=
|
ENSP00000262948.3:p.Gln391=
|
|
ENST00000394867.8:c.882G=
|
ENSP00000378336.1:p.Gln294=
|
|
ENST00000597263.5:n.358G=
|
|
|
ENST00000599021.1:c.283G=
|
|
|
ENST00000600584.5:n.2622G=
|
|
|
ENST00000601786.5:n.1474G=
|
|
|
NM_030662.3:c.1173G= , LRG_750t1:c.1173G=
|
NP_109587.1:p.Gln391=
|
|
XM_006722799.2:c.894G=
|
XP_006722862.1:p.Gln298=
|
|
XM_011528133.1:c.603G=
|
XP_011526435.1:p.Gln201=
|
|
NM_030662.4:c.1173G=
MANE Select
|
NP_109587.1:p.Gln391=
|
|