ENST00000355808.10:c.625G>T
|
ENSP00000348062.6:p.Gly209Cys
|
|
ENST00000379805.4:c.*296G>T
|
ENSP00000369133.3:n.*296G>T
|
|
ENST00000417819.6:c.688G>T
|
ENSP00000404616.2:p.Gly230Cys
|
|
ENST00000423505.6:c.718G>T
|
ENSP00000406473.2:p.Gly240Cys
|
|
ENST00000481733.2:n.399G>T
|
|
|
ENST00000696704.1:c.419G>T
|
ENSP00000512823.1:p.Gly140Val
|
|
ENST00000696705.1:c.*59G>T
|
ENSP00000512824.1:n.*59G>T
|
|
ENST00000422285.7:c.604G>T
MANE Select
|
ENSP00000394382.2:p.Gly202Cys
|
|
ENST00000379806.9:c.718G>T
|
ENSP00000369134.5:p.Gly240Cys
|
|
ENST00000422285.6:c.604G>T
|
ENSP00000394382.2:p.Gly202Cys
|
|
ENST00000479146.1:n.439G>T
|
|
|
ENST00000481733.1:n.32G>T
|
|
|
ENST00000540249.5:c.511G>T
|
ENSP00000440761.1:p.Gly171Cys
|
|
ENST00000545074.5:c.625G>T
|
ENSP00000438550.1:p.Gly209Cys
|
|
NM_000284.3:c.604G>T
|
NP_000275.1:p.Gly202Cys
|
|
NM_001173454.1:c.718G>T
|
NP_001166925.1:p.Gly240Cys
|
|
NM_001173455.1:c.625G>T
|
NP_001166926.1:p.Gly209Cys
|
|
NM_001173456.1:c.511G>T
|
NP_001166927.1:p.Gly171Cys
|
|
XM_011545531.1:c.739G>T
|
XP_011543833.1:p.Gly247Cys
|
|
XM_011545532.1:c.646G>T
|
XP_011543834.1:p.Gly216Cys
|
|
XM_017029574.2:c.625G>T
|
XP_016885063.1:p.Gly209Cys
|
|
NM_000284.4:c.604G>T
MANE Select
|
NP_000275.1:p.Gly202Cys
|
|
NM_001173454.2:c.718G>T
|
NP_001166925.1:p.Gly240Cys
|
|
NM_001173455.2:c.625G>T
|
NP_001166926.1:p.Gly209Cys
|
|
NM_001173456.2:c.511G>T
|
NP_001166927.1:p.Gly171Cys
|
|