ENST00000644719.2:c.207G>T
MANE Select
|
ENSP00000496625.1:p.Val69=
|
|
ENST00000418967.6:c.207G>T
|
ENSP00000408860.2:p.Val69=
|
|
ENST00000435122.3:c.202+102G>T
|
ENSP00000415043.2:n.202+102G>T
|
|
ENST00000464325.5:n.144G>T
|
|
|
ENST00000466779.5:c.207G>T
|
ENSP00000417321.1:p.Val69=
|
|
ENST00000469053.5:c.202+102G>T
|
ENSP00000418104.1:n.202+102G>T
|
|
ENST00000471671.4:c.207G>T
|
ENSP00000418561.1:p.Val69=
|
|
ENST00000478281.5:c.207G>T
|
ENSP00000419572.1:p.Val69=
|
|
ENST00000479074.5:n.265G>T
|
|
|
ENST00000479730.5:n.362G>T
|
|
|
ENST00000480027.1:n.260G>T
|
|
|
ENST00000483041.5:n.357G>T
|
|
|
ENST00000486063.5:n.387G>T
|
|
|
ENST00000488465.1:n.215G>T
|
|
|
NM_000500.7:c.207G>T
|
NP_000491.4:p.Val69=
|
|
NM_001128590.3:c.202+102G>T
|
NP_001122062.3:n.202+102G>T
|
|
XM_011514314.1:c.-218G>T
|
XP_011512616.1:n.-218G>T
|
|
NM_000500.9:c.207G>T
MANE Select
|
NP_000491.4:p.Val69=
|
|
NM_001368143.1:c.-218G>T
|
NP_001355072.1:n.-218G>T
|
|
NM_001368144.1:c.-133+102G>T
|
NP_001355073.1:n.-133+102G>T
|
|
NM_001128590.4:c.202+102G>T
|
NP_001122062.3:n.202+102G>T
|
|
NM_001368143.2:c.-218G>T
|
NP_001355072.1:n.-218G>T
|
|
NM_001368144.2:c.-133+102G>T
|
NP_001355073.1:n.-133+102G>T
|
|