ENST00000336079.8:c.752C>T
MANE Select
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ENSP00000336725.3:p.Ala251Val
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ENST00000336079.7:c.752C>T
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ENSP00000336725.3:p.Ala251Val
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ENST00000360160.8:c.752C>T
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ENSP00000353284.4:p.Ala251Val
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ENST00000440554.1:c.743C>T
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ENSP00000400377.1:p.Ala248Val
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ENST00000463199.1:n.270C>T
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ENST00000472510.5:n.315C>T
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NM_001122665.2:c.752C>T
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NP_001116137.1:p.Ala251Val
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NM_001302552.1:c.743C>T
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NP_001289481.1:p.Ala248Val
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NM_004660.4:c.752C>T
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NP_004651.2:p.Ala251Val
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XM_006724878.1:c.752C>T
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XP_006724941.1:p.Ala251Val
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XM_011531471.1:c.752C>T
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XP_011529773.1:p.Ala251Val
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NM_001122665.3:c.752C>T
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NP_001116137.1:p.Ala251Val
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NM_001302552.2:c.743C>T
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NP_001289481.1:p.Ala248Val
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NM_001324195.1:c.752C>T
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NP_001311124.1:p.Ala251Val
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NR_136716.1:n.903C>T
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NR_136717.1:n.983C>T
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NR_136718.1:n.983C>T
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NR_136719.1:n.773C>T
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NR_136720.1:n.903C>T
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NR_136721.1:n.831C>T
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NR_136722.1:n.898C>T
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NR_136723.1:n.898C>T
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NR_136724.1:n.818C>T
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XR_001756014.2:n.856C>T
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NM_004660.5:c.752C>T
MANE Select
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NP_004651.2:p.Ala251Val
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NM_001302552.3:c.743C>T
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NP_001289481.1:p.Ala248Val
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NM_001324195.2:c.752C>T
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NP_001311124.1:p.Ala251Val
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NR_136716.2:n.821C>T
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NR_136717.2:n.901C>T
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NR_136718.2:n.901C>T
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NR_136719.2:n.691C>T
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NR_136720.2:n.821C>T
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NR_136721.2:n.821C>T
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