ENST00000271651.8:c.512T>C
MANE Select
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ENSP00000271651.3:p.Val171Ala
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ENST00000443913.2:c.689T>C
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ENSP00000405083.2:p.Val230Ala
|
|
ENST00000480670.2:n.3581T>C
|
|
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ENST00000676680.1:c.512T>C
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ENSP00000503270.1:p.Val171Ala
|
|
ENST00000676716.1:c.389T>C
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ENSP00000504737.1:p.Val130Ala
|
|
ENST00000676751.1:c.512T>C
|
ENSP00000502964.1:p.Val171Ala
|
|
ENST00000676824.1:c.512T>C
|
ENSP00000504176.1:p.Val171Ala
|
|
ENST00000676966.1:c.512T>C
|
ENSP00000503723.1:p.Val171Ala
|
|
ENST00000676970.1:c.512T>C
|
ENSP00000503832.1:p.Val171Ala
|
|
ENST00000677330.1:n.2338T>C
|
|
|
ENST00000677611.1:n.364T>C
|
|
|
ENST00000677887.1:c.554T>C
|
ENSP00000503876.1:p.Val185Ala
|
|
ENST00000678275.1:c.*404T>C
|
ENSP00000504796.1:n.*404T>C
|
|
ENST00000678337.1:c.548T>C
|
ENSP00000504759.1:p.Val183Ala
|
|
ENST00000678725.1:n.1489T>C
|
|
|
ENST00000679090.1:n.1097T>C
|
|
|
ENST00000679148.1:n.3474T>C
|
|
|
ENST00000679171.1:n.2873T>C
|
|
|
ENST00000679260.1:c.399+1734T>C
|
ENSP00000504534.1:n.399+1734T>C
|
|
ENST00000271651.7:c.512T>C
|
ENSP00000271651.3:p.Val171Ala
|
|
ENST00000443913.1:c.689T>C
|
ENSP00000405083.1:p.Val230Ala
|
|
ENST00000480670.1:n.352T>C
|
|
|
NM_000396.3:c.512T>C
|
NP_000387.1:p.Val171Ala
|
|
NM_000396.4:c.512T>C
MANE Select
|
NP_000387.1:p.Val171Ala
|
|