|
ENST00000684779.1:c.541G=
|
ENSP00000508681.1:p.Glu181=
|
|
|
ENST00000685172.1:c.607G=
|
ENSP00000509604.1:p.Glu203=
|
|
|
ENST00000685763.1:c.460G=
|
ENSP00000509016.1:p.Glu154=
|
|
|
ENST00000686347.1:c.569-5435G=
|
ENSP00000509027.1:n.569-5435G=
|
|
|
ENST00000687191.1:n.965G=
|
|
|
|
ENST00000689951.1:c.658G=
|
ENSP00000509308.1:p.Glu220=
|
|
|
ENST00000691077.1:c.607G=
|
ENSP00000509843.1:p.Glu203=
|
|
|
ENST00000691576.1:c.569-3201G=
|
ENSP00000510066.1:n.569-3201G=
|
|
|
ENST00000691937.1:c.607G=
|
ENSP00000508768.1:p.Glu203=
|
|
|
ENST00000692487.1:c.607G=
|
ENSP00000509534.1:p.Glu203=
|
|
|
ENST00000692683.1:c.541G=
|
ENSP00000508437.1:p.Glu181=
|
|
|
ENST00000693150.1:c.463G=
|
ENSP00000510309.1:p.Glu155=
|
|
|
ENST00000307102.10:c.607G=
MANE Select
|
ENSP00000302486.5:p.Glu203=
|
|
|
ENST00000307102.9:c.607G=
|
ENSP00000302486.4:p.Glu203=
|
|
|
ENST00000566326.1:c.79G=
|
ENSP00000456438.1:p.Glu27=
|
|
|
NM_002755.3:c.607G= , LRG_725t1:c.607G=
|
NP_002746.1:p.Glu203=
|
|
|
XM_011521783.1:c.541G=
|
XP_011520085.1:p.Glu181=
|
|
|
XM_011521783.3:c.541G=
|
XP_011520085.1:p.Glu181=
|
|
|
XM_017022411.2:c.529G=
|
XP_016877900.1:p.Glu177=
|
|
|
XM_017022412.1:c.463G=
|
XP_016877901.1:p.Glu155=
|
|
|
XM_017022413.1:c.79G=
|
XP_016877902.1:p.Glu27=
|
|
|
NM_002755.4:c.607G=
MANE Select
|
NP_002746.1:p.Glu203=
|
|
