ENST00000271651.8:c.603C>G
MANE Select
|
ENSP00000271651.3:p.Tyr201Ter
|
|
ENST00000443913.2:c.780C>G
|
ENSP00000405083.2:p.Tyr260Ter
|
|
ENST00000480670.2:n.3672C>G
|
|
|
ENST00000676680.1:c.603C>G
|
ENSP00000503270.1:p.Tyr201Ter
|
|
ENST00000676716.1:c.480C>G
|
ENSP00000504737.1:p.Tyr160Ter
|
|
ENST00000676751.1:c.603C>G
|
ENSP00000502964.1:p.Tyr201Ter
|
|
ENST00000676824.1:c.603C>G
|
ENSP00000504176.1:p.Tyr201Ter
|
|
ENST00000676966.1:c.603C>G
|
ENSP00000503723.1:p.Tyr201Ter
|
|
ENST00000676970.1:c.603C>G
|
ENSP00000503832.1:p.Tyr201Ter
|
|
ENST00000677330.1:n.2429C>G
|
|
|
ENST00000677611.1:n.455C>G
|
|
|
ENST00000677887.1:c.645C>G
|
ENSP00000503876.1:p.Tyr215Ter
|
|
ENST00000678275.1:c.*495C>G
|
ENSP00000504796.1:n.*495C>G
|
|
ENST00000678337.1:c.639C>G
|
ENSP00000504759.1:p.Tyr213Ter
|
|
ENST00000678725.1:n.1580C>G
|
|
|
ENST00000679090.1:n.1188C>G
|
|
|
ENST00000679148.1:n.3565C>G
|
|
|
ENST00000679171.1:n.2964C>G
|
|
|
ENST00000679260.1:c.399+1825C>G
|
ENSP00000504534.1:n.399+1825C>G
|
|
ENST00000271651.7:c.603C>G
|
ENSP00000271651.3:p.Tyr201Ter
|
|
ENST00000480670.1:n.443C>G
|
|
|
NM_000396.3:c.603C>G
|
NP_000387.1:p.Tyr201Ter
|
|
NM_000396.4:c.603C>G
MANE Select
|
NP_000387.1:p.Tyr201Ter
|
|