ENST00000355808.10:c.644A>G
|
ENSP00000348062.6:p.Tyr215Cys
|
|
ENST00000379805.4:c.*315A>G
|
ENSP00000369133.3:n.*315A>G
|
|
ENST00000417819.6:c.707A>G
|
ENSP00000404616.2:p.Tyr236Cys
|
|
ENST00000423505.6:c.737A>G
|
ENSP00000406473.2:p.Tyr246Cys
|
|
ENST00000481733.2:n.418A>G
|
|
|
ENST00000696704.1:c.438A>G
|
ENSP00000512823.1:p.Leu146=
|
|
ENST00000696705.1:c.*78A>G
|
ENSP00000512824.1:n.*78A>G
|
|
ENST00000422285.7:c.623A>G
MANE Select
|
ENSP00000394382.2:p.Tyr208Cys
|
|
ENST00000379806.9:c.737A>G
|
ENSP00000369134.5:p.Tyr246Cys
|
|
ENST00000422285.6:c.623A>G
|
ENSP00000394382.2:p.Tyr208Cys
|
|
ENST00000479146.1:n.458A>G
|
|
|
ENST00000481733.1:n.51A>G
|
|
|
ENST00000540249.5:c.530A>G
|
ENSP00000440761.1:p.Tyr177Cys
|
|
ENST00000545074.5:c.644A>G
|
ENSP00000438550.1:p.Tyr215Cys
|
|
NM_000284.3:c.623A>G
|
NP_000275.1:p.Tyr208Cys
|
|
NM_001173454.1:c.737A>G
|
NP_001166925.1:p.Tyr246Cys
|
|
NM_001173455.1:c.644A>G
|
NP_001166926.1:p.Tyr215Cys
|
|
NM_001173456.1:c.530A>G
|
NP_001166927.1:p.Tyr177Cys
|
|
XM_011545531.1:c.758A>G
|
XP_011543833.1:p.Tyr253Cys
|
|
XM_011545532.1:c.665A>G
|
XP_011543834.1:p.Tyr222Cys
|
|
XM_017029574.2:c.644A>G
|
XP_016885063.1:p.Tyr215Cys
|
|
NM_000284.4:c.623A>G
MANE Select
|
NP_000275.1:p.Tyr208Cys
|
|
NM_001173454.2:c.737A>G
|
NP_001166925.1:p.Tyr246Cys
|
|
NM_001173455.2:c.644A>G
|
NP_001166926.1:p.Tyr215Cys
|
|
NM_001173456.2:c.530A>G
|
NP_001166927.1:p.Tyr177Cys
|
|