ENST00000219596.6:c.1553C>T
MANE Select
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ENSP00000219596.1:p.Ala518Val
|
|
ENST00000219596.5:c.1553C>T
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ENSP00000219596.1:p.Ala518Val
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|
ENST00000339854.8:c.1013C>T
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ENSP00000339639.4:p.Ala338Val
|
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ENST00000536379.5:c.920C>T
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ENSP00000445079.1:p.Ala307Val
|
|
ENST00000536980.5:c.920C>T
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ENSP00000444178.1:p.Ala307Val
|
|
ENST00000537682.5:c.1553C>T
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ENSP00000438611.1:p.Ala518Val
|
|
ENST00000538326.5:c.*178C>T
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ENSP00000437486.1:n.*178C>T
|
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ENST00000539145.5:c.474C>T
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ENSP00000444471.1:n.474C>T
|
|
ENST00000539154.1:n.918C>T
|
|
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ENST00000541159.5:c.920C>T
|
ENSP00000438711.1:p.Ala307Val
|
|
ENST00000542898.5:c.1646C>T
|
ENSP00000444615.1:p.Ala549Val
|
|
ENST00000570511.5:c.1107C>T
|
ENSP00000458312.1:n.1107C>T
|
|
ENST00000572244.5:c.278-503C>T
|
ENSP00000461186.1:n.278-503C>T
|
|
ENST00000574583.5:c.474C>T
|
ENSP00000460269.1:n.474C>T
|
|
ENST00000576315.5:c.474C>T
|
ENSP00000460551.1:n.474C>T
|
|
ENST00000621655.1:c.920C>T
|
ENSP00000481436.1:p.Ala307Val
|
|
NM_000243.2:c.1553C>T , LRG_190t1:c.1553C>T
|
NP_000234.1:p.Ala518Val
|
|
NM_001198536.1:c.920C>T
|
NP_001185465.1:p.Ala307Val
|
|
XM_017023236.2:c.1550C>T
|
XP_016878725.1:p.Ala517Val
|
|
XR_001751903.1:n.1742C>T
|
|
|
NM_000243.3:c.1553C>T
MANE Select
|
NP_000234.1:p.Ala518Val
|
|
NM_001198536.2:c.920C>T
|
NP_001185465.2:p.Ala307Val
|
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