ENST00000697124.1:n.733G=
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ENST00000219596.6:c.1612G=
MANE Select
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ENSP00000219596.1:p.Ala538=
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ENST00000219596.5:c.1612G=
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ENSP00000219596.1:p.Ala538=
|
|
ENST00000339854.8:c.1072G=
|
ENSP00000339639.4:p.Ala358=
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ENST00000536379.5:c.979G=
|
ENSP00000445079.1:p.Ala327=
|
|
ENST00000536980.5:c.979G=
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ENSP00000444178.1:p.Ala327=
|
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ENST00000537682.5:c.1612G=
|
ENSP00000438611.1:p.Ala538=
|
|
ENST00000538326.5:c.*237G=
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ENSP00000437486.1:n.*237G=
|
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ENST00000539145.5:c.533G=
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ENSP00000444471.1:n.533G=
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|
ENST00000541159.5:c.979G=
|
ENSP00000438711.1:p.Ala327=
|
|
ENST00000542898.5:c.1705G=
|
ENSP00000444615.1:p.Ala569=
|
|
ENST00000570511.5:c.1165-695G=
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ENSP00000458312.1:n.1165-695G=
|
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ENST00000572244.5:c.302G=
|
ENSP00000461186.1:p.Gly101=
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|
ENST00000574583.5:c.532-695G=
|
ENSP00000460269.1:n.532-695G=
|
|
ENST00000576315.5:c.532-301G=
|
ENSP00000460551.1:n.532-301G=
|
|
ENST00000621655.1:c.979G=
|
ENSP00000481436.1:p.Ala327=
|
|
NM_000243.2:c.1612G= , LRG_190t1:c.1612G=
|
NP_000234.1:p.Ala538=
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|
NM_001198536.1:c.979G=
|
NP_001185465.1:p.Ala327=
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|
XM_017023236.2:c.1609G=
|
XP_016878725.1:p.Ala537=
|
|
XR_001751903.1:n.1801G=
|
|
|
NM_000243.3:c.1612G=
MANE Select
|
NP_000234.1:p.Ala538=
|
|
NM_001198536.2:c.979G=
|
NP_001185465.2:p.Ala327=
|
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