ENST00000219596.6:c.1520C>G
MANE Select
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ENSP00000219596.1:p.Ala507Gly
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ENST00000219596.5:c.1520C>G
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ENSP00000219596.1:p.Ala507Gly
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ENST00000339854.8:c.980C>G
|
ENSP00000339639.4:p.Ala327Gly
|
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ENST00000536379.5:c.887C>G
|
ENSP00000445079.1:p.Ala296Gly
|
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ENST00000536980.5:c.887C>G
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ENSP00000444178.1:p.Ala296Gly
|
|
ENST00000537682.5:c.1520C>G
|
ENSP00000438611.1:p.Ala507Gly
|
|
ENST00000538326.5:c.*145C>G
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ENSP00000437486.1:n.*145C>G
|
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ENST00000539145.5:c.441C>G
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ENSP00000444471.1:n.441C>G
|
|
ENST00000539154.1:n.885C>G
|
|
|
ENST00000541159.5:c.887C>G
|
ENSP00000438711.1:p.Ala296Gly
|
|
ENST00000542898.5:c.1613C>G
|
ENSP00000444615.1:p.Ala538Gly
|
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ENST00000570511.5:c.1074C>G
|
ENSP00000458312.1:n.1074C>G
|
|
ENST00000572244.5:c.278-536C>G
|
ENSP00000461186.1:n.278-536C>G
|
|
ENST00000574583.5:c.441C>G
|
ENSP00000460269.1:n.441C>G
|
|
ENST00000576315.5:c.441C>G
|
ENSP00000460551.1:n.441C>G
|
|
ENST00000621655.1:c.887C>G
|
ENSP00000481436.1:p.Ala296Gly
|
|
NM_000243.2:c.1520C>G , LRG_190t1:c.1520C>G
|
NP_000234.1:p.Ala507Gly
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NM_001198536.1:c.887C>G
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NP_001185465.1:p.Ala296Gly
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|
XM_017023236.2:c.1517C>G
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XP_016878725.1:p.Ala506Gly
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XR_001751903.1:n.1709C>G
|
|
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NM_000243.3:c.1520C>G
MANE Select
|
NP_000234.1:p.Ala507Gly
|
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NM_001198536.2:c.887C>G
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NP_001185465.2:p.Ala296Gly
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