ENST00000557915.2:n.1214A>G
|
|
|
ENST00000557921.3:c.803A>G
|
ENSP00000453157.3:p.Glu268Gly
|
|
ENST00000699682.1:n.1301A>G
|
|
|
ENST00000699683.1:n.1351A>G
|
|
|
ENST00000699684.1:c.*504A>G
|
ENSP00000514523.1:n.*504A>G
|
|
ENST00000699685.1:n.1115A>G
|
|
|
ENST00000699686.1:c.704A>G
|
ENSP00000514524.1:p.Glu235Gly
|
|
ENST00000699687.1:c.806A>G
|
ENSP00000514525.1:p.Glu269Gly
|
|
ENST00000699688.1:n.1111A>G
|
|
|
ENST00000699689.1:n.1467A>G
|
|
|
ENST00000699690.1:n.1664A>G
|
|
|
ENST00000699691.1:n.1808A>G
|
|
|
ENST00000699693.1:n.1328A>G
|
|
|
ENST00000699694.1:n.1570A>G
|
|
|
ENST00000699695.1:c.*283A>G
|
ENSP00000514526.1:n.*283A>G
|
|
ENST00000699696.1:n.1214A>G
|
|
|
ENST00000699697.1:c.911A>G
|
ENSP00000514527.1:p.Glu304Gly
|
|
ENST00000699698.1:n.832A>G
|
|
|
ENST00000699699.1:n.1235A>G
|
|
|
ENST00000699700.1:n.1358A>G
|
|
|
ENST00000699701.1:c.*291A>G
|
ENSP00000514528.1:n.*291A>G
|
|
ENST00000267415.12:c.911A>G
MANE Select
|
ENSP00000267415.7:p.Glu304Gly
|
|
ENST00000557921.2:c.803A>G
|
ENSP00000453157.2:p.Glu268Gly
|
|
ENST00000646753.1:c.806A>G
|
ENSP00000494065.1:p.Glu269Gly
|
|
ENST00000267415.11:c.911A>G
|
ENSP00000267415.7:p.Glu304Gly
|
|
ENST00000399423.8:c.911A>G
|
ENSP00000382350.4:p.Glu304Gly
|
|
ENST00000557915.1:n.30A>G
|
|
|
ENST00000558566.1:c.*283A>G
|
ENSP00000453025.1:n.*283A>G
|
|
ENST00000559019.1:c.*283A>G
|
ENSP00000453675.1:n.*283A>G
|
|
ENST00000559969.5:c.758-89A>G
|
|
|
ENST00000626689.2:c.*283A>G
|
ENSP00000486681.1:n.*283A>G
|
|
NM_001099274.1:c.911A>G
|
NP_001092744.1:p.Glu304Gly
|
|
NM_012461.2:c.911A>G
|
NP_036593.2:p.Glu304Gly
|
|
XM_005267528.2:c.911A>G
|
XP_005267585.1:p.Glu304Gly
|
|
XM_005267529.2:c.806A>G
|
XP_005267586.1:p.Glu269Gly
|
|
NM_001099274.2:c.911A>G
|
NP_001092744.1:p.Glu304Gly
|
|
NM_001363668.1:c.806A>G
|
NP_001350597.1:p.Glu269Gly
|
|
NM_012461.3:c.911A>G
|
NP_036593.2:p.Glu304Gly
|
|
XM_011536642.2:c.*291A>G
|
XP_011534944.1:n.*291A>G
|
|
XM_017021216.2:c.269A>G
|
XP_016876705.1:p.Glu90Gly
|
|
XM_017021217.1:c.269A>G
|
XP_016876706.1:p.Glu90Gly
|
|
NM_001099274.3:c.911A>G
MANE Select
|
NP_001092744.1:p.Glu304Gly
|
|
NM_001363668.2:c.806A>G
|
NP_001350597.1:p.Glu269Gly
|
|