ENST00000355808.10:c.1016T>A
|
ENSP00000348062.6:p.Val339Glu
|
|
ENST00000379805.4:c.*687T>A
|
ENSP00000369133.3:n.*687T>A
|
|
ENST00000417819.6:c.1079T>A
|
ENSP00000404616.2:p.Val360Glu
|
|
ENST00000423505.6:c.1109T>A
|
ENSP00000406473.2:p.Val370Glu
|
|
ENST00000481733.2:n.790T>A
|
|
|
ENST00000696704.1:c.*327T>A
|
ENSP00000512823.1:n.*327T>A
|
|
ENST00000696705.1:c.*450T>A
|
ENSP00000512824.1:n.*450T>A
|
|
ENST00000422285.7:c.995T>A
MANE Select
|
ENSP00000394382.2:p.Val332Glu
|
|
ENST00000379804.1:c.152T>A
|
ENSP00000369132.1:p.Val51Glu
|
|
ENST00000379806.9:c.1109T>A
|
ENSP00000369134.5:p.Val370Glu
|
|
ENST00000422285.6:c.995T>A
|
ENSP00000394382.2:p.Val332Glu
|
|
ENST00000478795.1:n.434T>A
|
|
|
ENST00000481733.1:n.423T>A
|
|
|
ENST00000540249.5:c.902T>A
|
ENSP00000440761.1:p.Val301Glu
|
|
ENST00000545074.5:c.1016T>A
|
ENSP00000438550.1:p.Val339Glu
|
|
NM_000284.3:c.995T>A
|
NP_000275.1:p.Val332Glu
|
|
NM_001173454.1:c.1109T>A
|
NP_001166925.1:p.Val370Glu
|
|
NM_001173455.1:c.1016T>A
|
NP_001166926.1:p.Val339Glu
|
|
NM_001173456.1:c.902T>A
|
NP_001166927.1:p.Val301Glu
|
|
XM_011545531.1:c.1130T>A
|
XP_011543833.1:p.Val377Glu
|
|
XM_011545532.1:c.1037T>A
|
XP_011543834.1:p.Val346Glu
|
|
XM_017029574.2:c.1016T>A
|
XP_016885063.1:p.Val339Glu
|
|
NM_000284.4:c.995T>A
MANE Select
|
NP_000275.1:p.Val332Glu
|
|
NM_001173454.2:c.1109T>A
|
NP_001166925.1:p.Val370Glu
|
|
NM_001173455.2:c.1016T>A
|
NP_001166926.1:p.Val339Glu
|
|
NM_001173456.2:c.902T>A
|
NP_001166927.1:p.Val301Glu
|
|