ENST00000271651.8:c.420G>A
MANE Select
|
ENSP00000271651.3:p.Trp140Ter
|
|
ENST00000443913.2:c.597G>A
|
ENSP00000405083.2:p.Trp199Ter
|
|
ENST00000480670.2:n.3489G>A
|
|
|
ENST00000676680.1:c.420G>A
|
ENSP00000503270.1:p.Trp140Ter
|
|
ENST00000676716.1:c.297G>A
|
ENSP00000504737.1:p.Trp99Ter
|
|
ENST00000676751.1:c.420G>A
|
ENSP00000502964.1:p.Trp140Ter
|
|
ENST00000676824.1:c.420G>A
|
ENSP00000504176.1:p.Trp140Ter
|
|
ENST00000676966.1:c.420G>A
|
ENSP00000503723.1:p.Trp140Ter
|
|
ENST00000676970.1:c.420G>A
|
ENSP00000503832.1:p.Trp140Ter
|
|
ENST00000677330.1:n.2246G>A
|
|
|
ENST00000677611.1:n.272G>A
|
|
|
ENST00000677887.1:c.462G>A
|
ENSP00000503876.1:p.Trp154Ter
|
|
ENST00000678275.1:c.*312G>A
|
ENSP00000504796.1:n.*312G>A
|
|
ENST00000678337.1:c.456G>A
|
ENSP00000504759.1:p.Trp152Ter
|
|
ENST00000678725.1:n.1397G>A
|
|
|
ENST00000679090.1:n.1005G>A
|
|
|
ENST00000679148.1:n.3382G>A
|
|
|
ENST00000679171.1:n.2781G>A
|
|
|
ENST00000679260.1:c.399+1642G>A
|
ENSP00000504534.1:n.399+1642G>A
|
|
ENST00000271651.7:c.420G>A
|
ENSP00000271651.3:p.Trp140Ter
|
|
ENST00000443913.1:c.597G>A
|
ENSP00000405083.1:p.Trp199Ter
|
|
ENST00000480670.1:n.260G>A
|
|
|
NM_000396.3:c.420G>A
|
NP_000387.1:p.Trp140Ter
|
|
NM_000396.4:c.420G>A
MANE Select
|
NP_000387.1:p.Trp140Ter
|
|