ENST00000644719.2:c.294C>T
MANE Select
|
ENSP00000496625.1:p.Tyr98=
|
|
ENST00000418967.6:c.294C>T
|
ENSP00000408860.2:p.Tyr98=
|
|
ENST00000435122.3:c.204C>T
|
ENSP00000415043.2:p.Asp68=
|
|
ENST00000464325.5:n.230-15C>T
|
|
|
ENST00000466779.5:c.313C>T
|
ENSP00000417321.1:p.Gln105Ter
|
|
ENST00000466879.5:n.345C>T
|
|
|
ENST00000469053.5:c.223C>T
|
ENSP00000418104.1:p.Gln75Ter
|
|
ENST00000471671.4:c.294C>T
|
ENSP00000418561.1:p.Tyr98=
|
|
ENST00000478281.5:c.327C>T
|
ENSP00000419572.1:p.Asp109=
|
|
ENST00000479074.5:n.352C>T
|
|
|
ENST00000479730.5:n.449C>T
|
|
|
ENST00000480027.1:n.629C>T
|
|
|
ENST00000483041.5:n.463C>T
|
|
|
ENST00000486063.5:n.474C>T
|
|
|
ENST00000488465.1:n.302C>T
|
|
|
NM_000500.7:c.294C>T
|
NP_000491.4:p.Tyr98=
|
|
NM_001128590.3:c.204C>T
|
NP_001122062.3:p.Asp68=
|
|
XM_011514314.1:c.-112C>T
|
XP_011512616.1:n.-112C>T
|
|
NM_000500.9:c.294C>T
MANE Select
|
NP_000491.4:p.Tyr98=
|
|
NM_001368143.1:c.-112C>T
|
NP_001355072.1:n.-112C>T
|
|
NM_001368144.1:c.-112C>T
|
NP_001355073.1:n.-112C>T
|
|
NM_001128590.4:c.204C>T
|
NP_001122062.3:p.Asp68=
|
|
NM_001368143.2:c.-112C>T
|
NP_001355072.1:n.-112C>T
|
|
NM_001368144.2:c.-112C>T
|
NP_001355073.1:n.-112C>T
|
|