ENST00000644719.2:c.429G>C
MANE Select
|
ENSP00000496625.1:p.Leu143=
|
|
ENST00000418967.6:c.429G>C
|
ENSP00000408860.2:p.Leu143=
|
|
ENST00000435122.3:c.339G>C
|
ENSP00000415043.2:p.Leu113=
|
|
ENST00000462278.1:n.17G>C
|
|
|
ENST00000464325.5:n.350G>C
|
|
|
ENST00000466779.5:c.*121G>C
|
ENSP00000417321.1:n.*121G>C
|
|
ENST00000466879.5:n.480G>C
|
|
|
ENST00000469053.5:c.*121G>C
|
ENSP00000418104.1:n.*121G>C
|
|
ENST00000471671.4:c.429G>C
|
ENSP00000418561.1:p.Leu143=
|
|
ENST00000478281.5:c.462G>C
|
ENSP00000419572.1:p.Leu154=
|
|
ENST00000479074.5:n.487G>C
|
|
|
ENST00000479730.5:n.584G>C
|
|
|
ENST00000483041.5:n.598G>C
|
|
|
ENST00000486063.5:n.609G>C
|
|
|
ENST00000488465.1:n.437G>C
|
|
|
NM_000500.7:c.429G>C
|
NP_000491.4:p.Leu143=
|
|
NM_001128590.3:c.339G>C
|
NP_001122062.3:p.Leu113=
|
|
XM_011514314.1:c.24G>C
|
XP_011512616.1:p.Leu8=
|
|
NM_000500.9:c.429G>C
MANE Select
|
NP_000491.4:p.Leu143=
|
|
NM_001368143.1:c.24G>C
|
NP_001355072.1:p.Leu8=
|
|
NM_001368144.1:c.24G>C
|
NP_001355073.1:p.Leu8=
|
|
NM_001128590.4:c.339G>C
|
NP_001122062.3:p.Leu113=
|
|
NM_001368143.2:c.24G>C
|
NP_001355072.1:p.Leu8=
|
|
NM_001368144.2:c.24G>C
|
NP_001355073.1:p.Leu8=
|
|