ENST00000377270.8:c.294G>T
|
ENSP00000366482.4:p.Trp98Cys
|
|
ENST00000484259.3:c.519G>T
MANE Select
|
ENSP00000419243.2:p.Trp173Cys
|
|
ENST00000642330.1:c.384+19388G>T
|
ENSP00000493770.1:n.384+19388G>T
|
|
ENST00000642889.1:c.166-27253G>T
|
ENSP00000493780.1:n.166-27253G>T
|
|
ENST00000643352.1:c.482+7613G>T
|
ENSP00000496488.1:n.482+7613G>T
|
|
ENST00000643765.1:c.480+7613G>T
|
|
|
ENST00000644653.1:c.*122G>T
|
ENSP00000495217.1:n.*122G>T
|
|
ENST00000644977.1:c.*207+7613G>T
|
ENSP00000495651.1:n.*207+7613G>T
|
|
ENST00000645088.1:c.*85+7613G>T
|
ENSP00000495447.1:n.*85+7613G>T
|
|
ENST00000646862.1:c.384+19388G>T
|
ENSP00000494599.1:n.384+19388G>T
|
|
ENST00000377270.7:c.519G>T
|
ENSP00000366482.3:p.Trp173Cys
|
|
ENST00000396364.7:c.482+7613G>T
|
ENSP00000379650.3:n.482+7613G>T
|
|
ENST00000396366.6:c.527G>T
|
ENSP00000379652.2:p.Gly176Val
|
|
ENST00000484259.1:c.211G>T
|
|
|
ENST00000498653.5:c.294G>T
|
ENSP00000418015.1:p.Trp98Cys
|
|
NM_000144.4:c.519G>T
|
NP_000135.2:p.Trp173Cys
|
|
NM_001161706.1:c.482+7613G>T
|
NP_001155178.1:n.482+7613G>T
|
|
NM_181425.2:c.527G>T
|
NP_852090.1:p.Gly176Val
|
|
NM_000144.5:c.519G>T
MANE Select
|
NP_000135.2:p.Trp173Cys
|
|
NM_181425.3:c.527G>T
|
NP_852090.1:p.Gly176Val
|
|