ENST00000355808.10:c.687T>A
|
ENSP00000348062.6:p.Cys229Ter
|
|
ENST00000379805.4:c.*358T>A
|
ENSP00000369133.3:n.*358T>A
|
|
ENST00000417819.6:c.750T>A
|
ENSP00000404616.2:p.Cys250Ter
|
|
ENST00000423505.6:c.780T>A
|
ENSP00000406473.2:p.Cys260Ter
|
|
ENST00000481733.2:n.461T>A
|
|
|
ENST00000696704.1:c.481T>A
|
ENSP00000512823.1:p.Ter161Arg
|
|
ENST00000696705.1:c.*121T>A
|
ENSP00000512824.1:n.*121T>A
|
|
ENST00000422285.7:c.666T>A
MANE Select
|
ENSP00000394382.2:p.Cys222Ter
|
|
ENST00000379806.9:c.780T>A
|
ENSP00000369134.5:p.Cys260Ter
|
|
ENST00000422285.6:c.666T>A
|
ENSP00000394382.2:p.Cys222Ter
|
|
ENST00000479146.1:n.501T>A
|
|
|
ENST00000481733.1:n.94T>A
|
|
|
ENST00000540249.5:c.573T>A
|
ENSP00000440761.1:p.Cys191Ter
|
|
ENST00000545074.5:c.687T>A
|
ENSP00000438550.1:p.Cys229Ter
|
|
NM_000284.3:c.666T>A
|
NP_000275.1:p.Cys222Ter
|
|
NM_001173454.1:c.780T>A
|
NP_001166925.1:p.Cys260Ter
|
|
NM_001173455.1:c.687T>A
|
NP_001166926.1:p.Cys229Ter
|
|
NM_001173456.1:c.573T>A
|
NP_001166927.1:p.Cys191Ter
|
|
XM_011545531.1:c.801T>A
|
XP_011543833.1:p.Cys267Ter
|
|
XM_011545532.1:c.708T>A
|
XP_011543834.1:p.Cys236Ter
|
|
XM_017029574.2:c.687T>A
|
XP_016885063.1:p.Cys229Ter
|
|
NM_000284.4:c.666T>A
MANE Select
|
NP_000275.1:p.Cys222Ter
|
|
NM_001173454.2:c.780T>A
|
NP_001166925.1:p.Cys260Ter
|
|
NM_001173455.2:c.687T>A
|
NP_001166926.1:p.Cys229Ter
|
|
NM_001173456.2:c.573T>A
|
NP_001166927.1:p.Cys191Ter
|
|