|
NM_030662.4:c.546G>A
MANE Select
|
NP_109587.1:p.Ala182=
|
|
ENST00000262948.10:c.546G>A
MANE Select
|
ENSP00000262948.4:p.Ala182=
|
|
NM_030662.3:c.546G>A , LRG_750t1:c.546G>A
|
NP_109587.1:p.Ala182=
|
|
ENST00000262948.9:c.546G>A
|
ENSP00000262948.3:p.Ala182=
|
|
ENST00000394867.8:c.255G>A
|
ENSP00000378336.1:p.Ala85=
|
|
ENST00000394867.9:n.985G>A
|
|
|
ENST00000593364.5:n.493G>A
|
|
|
ENST00000597008.5:n.147G>A
|
|
|
ENST00000597263.5:n.10G>A
|
|
|
ENST00000599345.1:n.816G>A
|
|
|
ENST00000601786.5:n.847G>A
|
|
|
ENST00000602167.5:n.266G>A
|
|
|
ENST00000687128.1:n.985G>A
|
|
|
ENST00000689792.1:n.486G>A
|
|
|
XM_006722799.2:c.546G>A
|
XP_006722862.1:p.Ala182=
|
|
XM_011528133.1:c.-25G>A
|
XP_011526435.1:n.-25G>A
|
|
XM_017026989.1:c.546G>A
|
XP_016882478.1:p.Ala182=
|
|
XM_017026990.1:c.546G>A
|
XP_016882479.1:p.Ala182=
|
|
XM_017026991.1:c.546G>A
|
XP_016882480.1:p.Ala182=
|
