ENST00000271651.8:c.529T>A
MANE Select
|
ENSP00000271651.3:p.Cys177Ser
|
|
ENST00000443913.2:c.706T>A
|
ENSP00000405083.2:p.Cys236Ser
|
|
ENST00000480670.2:n.3598T>A
|
|
|
ENST00000676680.1:c.529T>A
|
ENSP00000503270.1:p.Cys177Ser
|
|
ENST00000676716.1:c.406T>A
|
ENSP00000504737.1:p.Cys136Ser
|
|
ENST00000676751.1:c.529T>A
|
ENSP00000502964.1:p.Cys177Ser
|
|
ENST00000676824.1:c.529T>A
|
ENSP00000504176.1:p.Cys177Ser
|
|
ENST00000676966.1:c.529T>A
|
ENSP00000503723.1:p.Cys177Ser
|
|
ENST00000676970.1:c.529T>A
|
ENSP00000503832.1:p.Cys177Ser
|
|
ENST00000677330.1:n.2355T>A
|
|
|
ENST00000677611.1:n.381T>A
|
|
|
ENST00000677887.1:c.571T>A
|
ENSP00000503876.1:p.Cys191Ser
|
|
ENST00000678275.1:c.*421T>A
|
ENSP00000504796.1:n.*421T>A
|
|
ENST00000678337.1:c.565T>A
|
ENSP00000504759.1:p.Cys189Ser
|
|
ENST00000678725.1:n.1506T>A
|
|
|
ENST00000679090.1:n.1114T>A
|
|
|
ENST00000679148.1:n.3491T>A
|
|
|
ENST00000679171.1:n.2890T>A
|
|
|
ENST00000679260.1:c.399+1751T>A
|
ENSP00000504534.1:n.399+1751T>A
|
|
ENST00000271651.7:c.529T>A
|
ENSP00000271651.3:p.Cys177Ser
|
|
ENST00000443913.1:c.706T>A
|
ENSP00000405083.1:p.Cys236Ser
|
|
ENST00000480670.1:n.369T>A
|
|
|
NM_000396.3:c.529T>A
|
NP_000387.1:p.Cys177Ser
|
|
NM_000396.4:c.529T>A
MANE Select
|
NP_000387.1:p.Cys177Ser
|
|