ENST00000219596.6:c.1519G>T
MANE Select
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ENSP00000219596.1:p.Ala507Ser
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ENST00000219596.5:c.1519G>T
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ENSP00000219596.1:p.Ala507Ser
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ENST00000339854.8:c.979G>T
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ENSP00000339639.4:p.Ala327Ser
|
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ENST00000536379.5:c.886G>T
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ENSP00000445079.1:p.Ala296Ser
|
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ENST00000536980.5:c.886G>T
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ENSP00000444178.1:p.Ala296Ser
|
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ENST00000537682.5:c.1519G>T
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ENSP00000438611.1:p.Ala507Ser
|
|
ENST00000538326.5:c.*144G>T
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ENSP00000437486.1:n.*144G>T
|
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ENST00000539145.5:c.440G>T
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ENSP00000444471.1:n.440G>T
|
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ENST00000539154.1:n.884G>T
|
|
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ENST00000541159.5:c.886G>T
|
ENSP00000438711.1:p.Ala296Ser
|
|
ENST00000542898.5:c.1612G>T
|
ENSP00000444615.1:p.Ala538Ser
|
|
ENST00000570511.5:c.1073G>T
|
ENSP00000458312.1:n.1073G>T
|
|
ENST00000572244.5:c.278-537G>T
|
ENSP00000461186.1:n.278-537G>T
|
|
ENST00000574583.5:c.440G>T
|
ENSP00000460269.1:n.440G>T
|
|
ENST00000576315.5:c.440G>T
|
ENSP00000460551.1:n.440G>T
|
|
ENST00000621655.1:c.886G>T
|
ENSP00000481436.1:p.Ala296Ser
|
|
NM_000243.2:c.1519G>T , LRG_190t1:c.1519G>T
|
NP_000234.1:p.Ala507Ser
|
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NM_001198536.1:c.886G>T
|
NP_001185465.1:p.Ala296Ser
|
|
XM_017023236.2:c.1516G>T
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XP_016878725.1:p.Ala506Ser
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|
XR_001751903.1:n.1708G>T
|
|
|
NM_000243.3:c.1519G>T
MANE Select
|
NP_000234.1:p.Ala507Ser
|
|
NM_001198536.2:c.886G>T
|
NP_001185465.2:p.Ala296Ser
|
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