ENST00000260361.9:c.343G>A
MANE Select
|
ENSP00000260361.4:p.Glu115Lys
|
|
ENST00000558719.2:c.343G>A
|
ENSP00000454083.2:p.Glu115Lys
|
|
ENST00000560978.2:c.343G>A
|
ENSP00000453944.2:p.Glu115Lys
|
|
ENST00000676533.1:c.343G>A
|
ENSP00000504040.1:p.Glu115Lys
|
|
ENST00000676906.1:c.-117G>A
|
ENSP00000503122.1:n.-117G>A
|
|
ENST00000677477.1:n.1569G>A
|
|
|
ENST00000678029.1:c.343G>A
|
ENSP00000503887.1:p.Glu115Lys
|
|
ENST00000678745.1:c.343G>A
|
ENSP00000503632.1:p.Glu115Lys
|
|
ENST00000679094.1:c.343G>A
|
ENSP00000504295.1:p.Glu115Lys
|
|
ENST00000679240.1:n.741G>A
|
|
|
ENST00000260361.8:c.343G>A
|
ENSP00000260361.4:p.Glu115Lys
|
|
ENST00000558719.1:c.343G>A
|
ENSP00000454083.1:p.Glu115Lys
|
|
ENST00000559127.5:c.343G>A
|
ENSP00000453027.1:p.Glu115Lys
|
|
ENST00000560978.1:c.343G>A
|
ENSP00000453944.1:p.Glu115Lys
|
|
NM_016013.3:c.343G>A
|
NP_057097.2:p.Glu115Lys
|
|
NR_045620.1:n.741G>A
|
|
|
XM_006720555.1:c.343G>A
|
XP_006720618.1:p.Glu115Lys
|
|
XM_011521658.1:c.343G>A
|
XP_011519960.1:p.Glu115Lys
|
|
XM_011521659.1:c.343G>A
|
XP_011519961.1:p.Glu115Lys
|
|
XM_006720555.3:c.343G>A
|
XP_006720618.1:p.Glu115Lys
|
|
XM_011521659.3:c.343G>A
|
XP_011519961.1:p.Glu115Lys
|
|
XM_024449945.1:c.343G>A
|
XP_024305713.1:p.Glu115Lys
|
|
NM_016013.4:c.343G>A
MANE Select
|
NP_057097.2:p.Glu115Lys
|
|
NR_045620.2:n.777G>A
|
|
|