|
NM_001754.5:c.1338C>A
MANE Select
|
NP_001745.2:p.Leu446=
|
|
ENST00000675419.1:c.1338C>A
MANE Select
|
ENSP00000501943.1:p.Leu446=
|
|
NM_001001890.2:c.1257C>A
|
NP_001001890.1:p.Leu419=
|
|
NM_001001890.3:c.1257C>A
|
NP_001001890.1:p.Leu419=
|
|
NM_001754.4:c.1338C>A , LRG_482t1:c.1338C>A
|
NP_001745.2:p.Leu446=
|
|
ENST00000300305.7:c.1338C>A
|
ENSP00000300305.3:p.Leu446=
|
|
ENST00000344691.8:c.1257C>A
|
ENSP00000340690.4:p.Leu419=
|
|
ENST00000399240.5:c.1065C>A
|
ENSP00000382184.1:p.Leu355=
|
|
ENST00000437180.5:c.1338C>A
|
ENSP00000409227.1:p.Leu446=
|
|
ENST00000482318.5:c.*928C>A
|
ENSP00000477067.1:n.*928C>A
|
|
XM_005261068.3:c.1302C>A
|
XP_005261125.1:p.Leu434=
|
|
XM_005261069.3:c.1146C>A
|
XP_005261126.1:p.Leu382=
|
|
XM_005261069.4:c.1146C>A
|
XP_005261126.1:p.Leu382=
|
|
XM_011529766.1:c.1338C>A
|
XP_011528068.1:p.Leu446=
|
|
XM_011529766.2:c.1338C>A
|
XP_011528068.1:p.Leu446=
|
|
XM_011529767.1:c.1299C>A
|
XP_011528069.1:p.Leu433=
|
|
XM_011529767.2:c.1299C>A
|
XP_011528069.1:p.Leu433=
|
|
XM_011529768.1:c.1107C>A
|
XP_011528070.1:p.Leu369=
|
|
XM_011529768.2:c.1107C>A
|
XP_011528070.1:p.Leu369=
|
|
XM_017028487.1:c.1185C>A
|
XP_016883976.1:p.Leu395=
|
