ENST00000697149.1:c.1513C>A
|
ENSP00000513138.1:n.1513C>A
|
|
ENST00000697150.1:c.1571C>A
|
ENSP00000513139.1:n.1571C>A
|
|
ENST00000697151.1:c.1504C>A
|
ENSP00000513140.1:n.1504C>A
|
|
ENST00000697164.1:c.1584C>A
|
ENSP00000513153.1:p.Cys528Ter
|
|
ENST00000697165.1:c.1371C>A
|
ENSP00000513154.1:p.Cys457Ter
|
|
ENST00000347310.10:c.1674C>A
MANE Select
|
ENSP00000321345.5:p.Cys558Ter
|
|
ENST00000637002.1:c.1065C>A
|
ENSP00000490340.1:p.Cys355Ter
|
|
ENST00000347310.9:c.1674C>A
|
ENSP00000321345.5:p.Cys558Ter
|
|
ENST00000395227.2:c.468C>A
|
ENSP00000378652.2:p.Cys156Ter
|
|
ENST00000425614.3:c.909C>A
|
ENSP00000387640.2:p.Cys303Ter
|
|
ENST00000473881.2:c.*500C>A
|
ENSP00000486667.1:n.*500C>A
|
|
NM_144701.2:c.1674C>A
|
NP_653302.2:p.Cys558Ter
|
|
XM_005270516.2:c.912C>A
|
XP_005270573.1:p.Cys304Ter
|
|
XM_011540789.1:c.1764C>A
|
XP_011539091.1:p.Cys588Ter
|
|
XM_011540790.1:c.1674C>A
|
XP_011539092.1:p.Cys558Ter
|
|
XM_011540791.1:c.1674C>A
|
XP_011539093.1:p.Cys558Ter
|
|
XM_011540790.3:c.1674C>A
|
XP_011539092.1:p.Cys558Ter
|
|
XM_011540791.3:c.1674C>A
|
XP_011539093.1:p.Cys558Ter
|
|
XR_001736993.1:n.1754C>A
|
|
|
NM_144701.3:c.1674C>A
MANE Select
|
NP_653302.2:p.Cys558Ter
|
|