ENST00000271651.8:c.609T>G
MANE Select
|
ENSP00000271651.3:p.Tyr203Ter
|
|
ENST00000443913.2:c.786T>G
|
ENSP00000405083.2:p.Tyr262Ter
|
|
ENST00000480670.2:n.3678T>G
|
|
|
ENST00000676680.1:c.609T>G
|
ENSP00000503270.1:p.Tyr203Ter
|
|
ENST00000676716.1:c.486T>G
|
ENSP00000504737.1:p.Tyr162Ter
|
|
ENST00000676751.1:c.609T>G
|
ENSP00000502964.1:p.Tyr203Ter
|
|
ENST00000676824.1:c.609T>G
|
ENSP00000504176.1:p.Tyr203Ter
|
|
ENST00000676966.1:c.609T>G
|
ENSP00000503723.1:p.Tyr203Ter
|
|
ENST00000676970.1:c.609T>G
|
ENSP00000503832.1:p.Tyr203Ter
|
|
ENST00000677330.1:n.2435T>G
|
|
|
ENST00000677611.1:n.461T>G
|
|
|
ENST00000677887.1:c.651T>G
|
ENSP00000503876.1:p.Tyr217Ter
|
|
ENST00000678275.1:c.*501T>G
|
ENSP00000504796.1:n.*501T>G
|
|
ENST00000678337.1:c.645T>G
|
ENSP00000504759.1:p.Tyr215Ter
|
|
ENST00000678725.1:n.1586T>G
|
|
|
ENST00000679090.1:n.1194T>G
|
|
|
ENST00000679148.1:n.3571T>G
|
|
|
ENST00000679171.1:n.2970T>G
|
|
|
ENST00000679260.1:c.399+1831T>G
|
ENSP00000504534.1:n.399+1831T>G
|
|
ENST00000271651.7:c.609T>G
|
ENSP00000271651.3:p.Tyr203Ter
|
|
ENST00000480670.1:n.449T>G
|
|
|
NM_000396.3:c.609T>G
|
NP_000387.1:p.Tyr203Ter
|
|
NM_000396.4:c.609T>G
MANE Select
|
NP_000387.1:p.Tyr203Ter
|
|