ENST00000271651.8:c.510T>A
MANE Select
|
ENSP00000271651.3:p.Cys170Ter
|
|
ENST00000443913.2:c.687T>A
|
ENSP00000405083.2:p.Cys229Ter
|
|
ENST00000480670.2:n.3579T>A
|
|
|
ENST00000676680.1:c.510T>A
|
ENSP00000503270.1:p.Cys170Ter
|
|
ENST00000676716.1:c.387T>A
|
ENSP00000504737.1:p.Cys129Ter
|
|
ENST00000676751.1:c.510T>A
|
ENSP00000502964.1:p.Cys170Ter
|
|
ENST00000676824.1:c.510T>A
|
ENSP00000504176.1:p.Cys170Ter
|
|
ENST00000676966.1:c.510T>A
|
ENSP00000503723.1:p.Cys170Ter
|
|
ENST00000676970.1:c.510T>A
|
ENSP00000503832.1:p.Cys170Ter
|
|
ENST00000677330.1:n.2336T>A
|
|
|
ENST00000677611.1:n.362T>A
|
|
|
ENST00000677887.1:c.552T>A
|
ENSP00000503876.1:p.Cys184Ter
|
|
ENST00000678275.1:c.*402T>A
|
ENSP00000504796.1:n.*402T>A
|
|
ENST00000678337.1:c.546T>A
|
ENSP00000504759.1:p.Cys182Ter
|
|
ENST00000678725.1:n.1487T>A
|
|
|
ENST00000679090.1:n.1095T>A
|
|
|
ENST00000679148.1:n.3472T>A
|
|
|
ENST00000679171.1:n.2871T>A
|
|
|
ENST00000679260.1:c.399+1732T>A
|
ENSP00000504534.1:n.399+1732T>A
|
|
ENST00000271651.7:c.510T>A
|
ENSP00000271651.3:p.Cys170Ter
|
|
ENST00000443913.1:c.687T>A
|
ENSP00000405083.1:p.Cys229Ter
|
|
ENST00000480670.1:n.350T>A
|
|
|
NM_000396.3:c.510T>A
|
NP_000387.1:p.Cys170Ter
|
|
NM_000396.4:c.510T>A
MANE Select
|
NP_000387.1:p.Cys170Ter
|
|