ENST00000336079.8:c.763A>C
MANE Select
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ENSP00000336725.3:p.Asn255His
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ENST00000336079.7:c.763A>C
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ENSP00000336725.3:p.Asn255His
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ENST00000360160.8:c.763A>C
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ENSP00000353284.4:p.Asn255His
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ENST00000463199.1:n.281A>C
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|
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ENST00000472510.5:n.560A>C
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NM_001122665.2:c.763A>C
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NP_001116137.1:p.Asn255His
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NM_001302552.1:c.754A>C
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NP_001289481.1:p.Asn252His
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NM_004660.4:c.763A>C
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NP_004651.2:p.Asn255His
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XM_006724878.1:c.763A>C
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XP_006724941.1:p.Asn255His
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XM_011531471.1:c.763A>C
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XP_011529773.1:p.Asn255His
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NM_001122665.3:c.763A>C
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NP_001116137.1:p.Asn255His
|
|
NM_001302552.2:c.754A>C
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NP_001289481.1:p.Asn252His
|
|
NM_001324195.1:c.763A>C
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NP_001311124.1:p.Asn255His
|
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NR_136716.1:n.1148A>C
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|
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NR_136717.1:n.994A>C
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|
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NR_136718.1:n.1228A>C
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NR_136719.1:n.1018A>C
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NR_136720.1:n.1148A>C
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|
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NR_136721.1:n.842A>C
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|
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NR_136722.1:n.909A>C
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|
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NR_136723.1:n.1143A>C
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|
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NR_136724.1:n.1063A>C
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|
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XR_001756014.2:n.867A>C
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|
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NM_004660.5:c.763A>C
MANE Select
|
NP_004651.2:p.Asn255His
|
|
NM_001302552.3:c.754A>C
|
NP_001289481.1:p.Asn252His
|
|
NM_001324195.2:c.763A>C
|
NP_001311124.1:p.Asn255His
|
|
NR_136716.2:n.1066A>C
|
|
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NR_136717.2:n.912A>C
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|
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NR_136718.2:n.1146A>C
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|
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NR_136719.2:n.936A>C
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|
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NR_136720.2:n.1066A>C
|
|
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NR_136721.2:n.832A>C
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