ENST00000355808.10:c.687T>G
|
ENSP00000348062.6:p.Cys229Trp
|
|
ENST00000379805.4:c.*358T>G
|
ENSP00000369133.3:n.*358T>G
|
|
ENST00000417819.6:c.750T>G
|
ENSP00000404616.2:p.Cys250Trp
|
|
ENST00000423505.6:c.780T>G
|
ENSP00000406473.2:p.Cys260Trp
|
|
ENST00000481733.2:n.461T>G
|
|
|
ENST00000696704.1:c.481T>G
|
ENSP00000512823.1:p.Ter161Gly
|
|
ENST00000696705.1:c.*121T>G
|
ENSP00000512824.1:n.*121T>G
|
|
ENST00000422285.7:c.666T>G
MANE Select
|
ENSP00000394382.2:p.Cys222Trp
|
|
ENST00000379806.9:c.780T>G
|
ENSP00000369134.5:p.Cys260Trp
|
|
ENST00000422285.6:c.666T>G
|
ENSP00000394382.2:p.Cys222Trp
|
|
ENST00000479146.1:n.501T>G
|
|
|
ENST00000481733.1:n.94T>G
|
|
|
ENST00000540249.5:c.573T>G
|
ENSP00000440761.1:p.Cys191Trp
|
|
ENST00000545074.5:c.687T>G
|
ENSP00000438550.1:p.Cys229Trp
|
|
NM_000284.3:c.666T>G
|
NP_000275.1:p.Cys222Trp
|
|
NM_001173454.1:c.780T>G
|
NP_001166925.1:p.Cys260Trp
|
|
NM_001173455.1:c.687T>G
|
NP_001166926.1:p.Cys229Trp
|
|
NM_001173456.1:c.573T>G
|
NP_001166927.1:p.Cys191Trp
|
|
XM_011545531.1:c.801T>G
|
XP_011543833.1:p.Cys267Trp
|
|
XM_011545532.1:c.708T>G
|
XP_011543834.1:p.Cys236Trp
|
|
XM_017029574.2:c.687T>G
|
XP_016885063.1:p.Cys229Trp
|
|
NM_000284.4:c.666T>G
MANE Select
|
NP_000275.1:p.Cys222Trp
|
|
NM_001173454.2:c.780T>G
|
NP_001166925.1:p.Cys260Trp
|
|
NM_001173455.2:c.687T>G
|
NP_001166926.1:p.Cys229Trp
|
|
NM_001173456.2:c.573T>G
|
NP_001166927.1:p.Cys191Trp
|
|