ENST00000397195.10:c.662T>C
MANE Select
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ENSP00000380378.4:p.Val221Ala
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ENST00000571495.2:n.445T>C
|
|
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ENST00000674608.1:c.716T>C
|
ENSP00000501976.1:p.Val239Ala
|
|
ENST00000674717.1:c.467T>C
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ENSP00000501931.1:p.Val156Ala
|
|
ENST00000675202.1:c.662T>C
|
ENSP00000502843.1:p.Val221Ala
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|
ENST00000675331.1:c.662T>C
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ENSP00000502031.1:p.Val221Ala
|
|
ENST00000675390.1:c.662T>C
|
ENSP00000501969.1:p.Val221Ala
|
|
ENST00000675574.1:n.432T>C
|
|
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ENST00000675621.1:c.662T>C
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ENSP00000502117.1:p.Val221Ala
|
|
ENST00000675764.1:c.*616T>C
|
ENSP00000502242.1:n.*616T>C
|
|
ENST00000676077.1:c.374-1312T>C
|
ENSP00000502507.1:n.374-1312T>C
|
|
ENST00000676098.1:c.662T>C
|
ENSP00000502735.1:p.Val221Ala
|
|
ENST00000676188.1:c.662T>C
|
ENSP00000502577.1:p.Val221Ala
|
|
ENST00000676353.1:c.467T>C
|
ENSP00000502737.1:p.Val156Ala
|
|
ENST00000397193.7:n.470T>C
|
|
|
ENST00000397195.9:c.662T>C
|
ENSP00000380378.4:p.Val221Ala
|
|
ENST00000572915.6:n.630T>C
|
|
|
ENST00000574468.1:c.158T>C
|
ENSP00000460591.1:p.Val53Ala
|
|
ENST00000574816.5:n.31-3566T>C
|
|
|
NM_000430.3:c.662T>C
|
NP_000421.1:p.Val221Ala
|
|
XM_011523901.1:c.716T>C
|
XP_011522203.1:p.Val239Ala
|
|
XM_011523902.1:c.716T>C
|
XP_011522204.1:p.Val239Ala
|
|
XM_011523903.1:c.716T>C
|
XP_011522205.1:p.Val239Ala
|
|
XM_011523904.1:c.623-1312T>C
|
XP_011522206.1:n.623-1312T>C
|
|
XM_011523901.2:c.716T>C
|
XP_011522203.1:p.Val239Ala
|
|
XM_011523902.3:c.716T>C
|
XP_011522204.1:p.Val239Ala
|
|
XM_011523903.2:c.716T>C
|
XP_011522205.1:p.Val239Ala
|
|
XM_017024701.1:c.662T>C
|
XP_016880190.1:p.Val221Ala
|
|
XM_017024702.2:c.467T>C
|
XP_016880191.1:p.Val156Ala
|
|
NM_000430.4:c.662T>C
MANE Select
|
NP_000421.1:p.Val221Ala
|
|