ENST00000271651.8:c.539G>A
MANE Select
|
ENSP00000271651.3:p.Gly180Asp
|
|
ENST00000443913.2:c.716G>A
|
ENSP00000405083.2:p.Gly239Asp
|
|
ENST00000480670.2:n.3608G>A
|
|
|
ENST00000676680.1:c.539G>A
|
ENSP00000503270.1:p.Gly180Asp
|
|
ENST00000676716.1:c.416G>A
|
ENSP00000504737.1:p.Gly139Asp
|
|
ENST00000676751.1:c.539G>A
|
ENSP00000502964.1:p.Gly180Asp
|
|
ENST00000676824.1:c.539G>A
|
ENSP00000504176.1:p.Gly180Asp
|
|
ENST00000676966.1:c.539G>A
|
ENSP00000503723.1:p.Gly180Asp
|
|
ENST00000676970.1:c.539G>A
|
ENSP00000503832.1:p.Gly180Asp
|
|
ENST00000677330.1:n.2365G>A
|
|
|
ENST00000677611.1:n.391G>A
|
|
|
ENST00000677887.1:c.581G>A
|
ENSP00000503876.1:p.Gly194Asp
|
|
ENST00000678275.1:c.*431G>A
|
ENSP00000504796.1:n.*431G>A
|
|
ENST00000678337.1:c.575G>A
|
ENSP00000504759.1:p.Gly192Asp
|
|
ENST00000678725.1:n.1516G>A
|
|
|
ENST00000679090.1:n.1124G>A
|
|
|
ENST00000679148.1:n.3501G>A
|
|
|
ENST00000679171.1:n.2900G>A
|
|
|
ENST00000679260.1:c.399+1761G>A
|
ENSP00000504534.1:n.399+1761G>A
|
|
ENST00000271651.7:c.539G>A
|
ENSP00000271651.3:p.Gly180Asp
|
|
ENST00000443913.1:c.716G>A
|
ENSP00000405083.1:p.Gly239Asp
|
|
ENST00000480670.1:n.379G>A
|
|
|
NM_000396.3:c.539G>A
|
NP_000387.1:p.Gly180Asp
|
|
NM_000396.4:c.539G>A
MANE Select
|
NP_000387.1:p.Gly180Asp
|
|