ENST00000271651.8:c.402T>C
MANE Select
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ENSP00000271651.3:p.Gly134=
|
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ENST00000443913.2:c.579T>C
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ENSP00000405083.2:p.Gly193=
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ENST00000480670.2:n.3471T>C
|
|
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ENST00000676680.1:c.402T>C
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ENSP00000503270.1:p.Gly134=
|
|
ENST00000676716.1:c.279T>C
|
ENSP00000504737.1:p.Gly93=
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|
ENST00000676751.1:c.402T>C
|
ENSP00000502964.1:p.Gly134=
|
|
ENST00000676824.1:c.402T>C
|
ENSP00000504176.1:p.Gly134=
|
|
ENST00000676966.1:c.402T>C
|
ENSP00000503723.1:p.Gly134=
|
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ENST00000676970.1:c.402T>C
|
ENSP00000503832.1:p.Gly134=
|
|
ENST00000677330.1:n.2228T>C
|
|
|
ENST00000677611.1:n.254T>C
|
|
|
ENST00000677887.1:c.444T>C
|
ENSP00000503876.1:p.Gly148=
|
|
ENST00000678275.1:c.*294T>C
|
ENSP00000504796.1:n.*294T>C
|
|
ENST00000678337.1:c.438T>C
|
ENSP00000504759.1:p.Gly146=
|
|
ENST00000678725.1:n.1379T>C
|
|
|
ENST00000679090.1:n.987T>C
|
|
|
ENST00000679148.1:n.3364T>C
|
|
|
ENST00000679171.1:n.2763T>C
|
|
|
ENST00000679260.1:c.399+1624T>C
|
ENSP00000504534.1:n.399+1624T>C
|
|
ENST00000271651.7:c.402T>C
|
ENSP00000271651.3:p.Gly134=
|
|
ENST00000443913.1:c.579T>C
|
ENSP00000405083.1:p.Gly193=
|
|
ENST00000480670.1:n.242T>C
|
|
|
NM_000396.3:c.402T>C
|
NP_000387.1:p.Gly134=
|
|
NM_000396.4:c.402T>C
MANE Select
|
NP_000387.1:p.Gly134=
|
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