ENST00000295897.9:c.876A>C
MANE Select
|
ENSP00000295897.4:p.Gln292His
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|
ENST00000295897.8:c.876A>C
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ENSP00000295897.4:p.Gln292His
|
|
ENST00000401494.7:c.531A>C
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ENSP00000384695.3:p.Gln177His
|
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ENST00000415165.6:c.300A>C
|
ENSP00000401820.2:p.Gln100His
|
|
ENST00000476441.6:c.*155A>C
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ENSP00000423727.1:n.*155A>C
|
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ENST00000484992.1:n.196A>C
|
|
|
ENST00000503124.5:c.426A>C
|
ENSP00000421027.1:p.Gln142His
|
|
ENST00000505649.5:n.562A>C
|
|
|
ENST00000509063.5:c.876A>C
|
ENSP00000422784.1:p.Gln292His
|
|
ENST00000511370.1:c.409A>C
|
|
|
ENST00000621085.4:c.491-1654A>C
|
ENSP00000483421.1:n.491-1654A>C
|
|
ENST00000621628.4:c.487-1650A>C
|
ENSP00000480485.1:n.487-1650A>C
|
|
NM_000477.5:c.876A>C
|
NP_000468.1:p.Gln292His
|
|
NM_000477.6:c.876A>C
|
NP_000468.1:p.Gln292His
|
|
NM_000477.7:c.876A>C
MANE Select
|
NP_000468.1:p.Gln292His
|
|