ENST00000435817.7:c.798T>C
MANE Select
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ENSP00000399259.2:p.His266=
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ENST00000435817.6:c.798T>C
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ENSP00000399259.2:p.His266=
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ENST00000522126.5:c.570T>C
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ENSP00000427796.1:p.His190=
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ENST00000522386.1:n.404T>C
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ENST00000522763.5:n.102T>C
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ENST00000522783.5:c.792T>C
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ENSP00000428677.1:p.His264=
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ENST00000523856.5:n.56T>C
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NM_033449.2:c.798T>C
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NP_258260.1:p.His266=
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XM_005268524.3:c.792T>C
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XP_005268581.1:p.His264=
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XM_006714803.2:c.669T>C
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XP_006714866.1:p.His223=
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XM_011537698.1:c.798T>C
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XP_011536000.1:p.His266=
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XM_011537699.1:c.798T>C
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XP_011536001.1:p.His266=
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XM_011537700.1:c.798T>C
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XP_011536002.1:p.His266=
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XM_011537701.1:c.798T>C
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XP_011536003.1:p.His266=
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XR_427781.2:n.852T>C
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XR_944338.1:n.858T>C
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XR_944339.1:n.858T>C
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XM_005268524.5:c.792T>C
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XP_005268581.1:p.His264=
|
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XM_006714803.4:c.669T>C
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XP_006714866.1:p.His223=
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XM_011537698.3:c.798T>C
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XP_011536000.1:p.His266=
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XM_011537700.3:c.798T>C
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XP_011536002.1:p.His266=
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XM_011537701.3:c.798T>C
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XP_011536003.1:p.His266=
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XM_017010013.2:c.798T>C
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XP_016865502.1:p.His266=
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XR_002956197.1:n.794T>C
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XR_427781.4:n.794T>C
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XR_944338.3:n.873T>C
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XR_944339.3:n.873T>C
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NM_033449.3:c.798T>C
MANE Select
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NP_258260.1:p.His266=
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