ENST00000355808.10:c.893G>A
|
ENSP00000348062.6:p.Gly298Glu
|
|
ENST00000379805.4:c.*564G>A
|
ENSP00000369133.3:n.*564G>A
|
|
ENST00000417819.6:c.956G>A
|
ENSP00000404616.2:p.Gly319Glu
|
|
ENST00000423505.6:c.986G>A
|
ENSP00000406473.2:p.Gly329Glu
|
|
ENST00000481733.2:n.667G>A
|
|
|
ENST00000696704.1:c.*204G>A
|
ENSP00000512823.1:n.*204G>A
|
|
ENST00000696705.1:c.*327G>A
|
ENSP00000512824.1:n.*327G>A
|
|
ENST00000422285.7:c.872G>A
MANE Select
|
ENSP00000394382.2:p.Gly291Glu
|
|
ENST00000379804.1:c.29G>A
|
ENSP00000369132.1:p.Gly10Glu
|
|
ENST00000379806.9:c.986G>A
|
ENSP00000369134.5:p.Gly329Glu
|
|
ENST00000422285.6:c.872G>A
|
ENSP00000394382.2:p.Gly291Glu
|
|
ENST00000478795.1:n.311G>A
|
|
|
ENST00000481733.1:n.300G>A
|
|
|
ENST00000540249.5:c.779G>A
|
ENSP00000440761.1:p.Gly260Glu
|
|
ENST00000545074.5:c.893G>A
|
ENSP00000438550.1:p.Gly298Glu
|
|
NM_000284.3:c.872G>A
|
NP_000275.1:p.Gly291Glu
|
|
NM_001173454.1:c.986G>A
|
NP_001166925.1:p.Gly329Glu
|
|
NM_001173455.1:c.893G>A
|
NP_001166926.1:p.Gly298Glu
|
|
NM_001173456.1:c.779G>A
|
NP_001166927.1:p.Gly260Glu
|
|
XM_011545531.1:c.1007G>A
|
XP_011543833.1:p.Gly336Glu
|
|
XM_011545532.1:c.914G>A
|
XP_011543834.1:p.Gly305Glu
|
|
XM_017029574.2:c.893G>A
|
XP_016885063.1:p.Gly298Glu
|
|
NM_000284.4:c.872G>A
MANE Select
|
NP_000275.1:p.Gly291Glu
|
|
NM_001173454.2:c.986G>A
|
NP_001166925.1:p.Gly329Glu
|
|
NM_001173455.2:c.893G>A
|
NP_001166926.1:p.Gly298Glu
|
|
NM_001173456.2:c.779G>A
|
NP_001166927.1:p.Gly260Glu
|
|