ENST00000588860.6:c.1527G=
|
ENSP00000465878.2:p.Trp509=
|
|
ENST00000589076.6:c.1527G=
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ENSP00000466934.2:p.Trp509=
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ENST00000589941.2:c.1527G=
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ENSP00000465874.2:p.Trp509=
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|
ENST00000590061.2:c.1527G=
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ENSP00000464772.2:p.Trp509=
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ENST00000593223.2:c.*1524G=
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ENSP00000466118.2:n.*1524G=
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|
ENST00000611848.2:c.*179G=
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ENSP00000478613.2:n.*179G=
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ENST00000684953.1:n.3542G=
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|
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ENST00000685090.1:n.3457G=
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|
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ENST00000685232.1:n.1748G=
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|
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ENST00000688574.1:n.1635G=
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|
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ENST00000691124.1:n.4488G=
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|
|
ENST00000342988.8:c.1527G=
MANE Select
|
ENSP00000341551.3:p.Trp509=
|
|
ENST00000342988.7:c.1527G=
|
ENSP00000341551.3:p.Trp509=
|
|
ENST00000398417.6:c.1527G=
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ENSP00000381452.1:p.Trp509=
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|
ENST00000586253.1:n.249G=
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|
|
ENST00000588745.5:c.1239G=
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ENSP00000464901.1:p.Trp413=
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|
ENST00000591126.5:n.3528G=
|
|
|
ENST00000592186.5:c.1174G=
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ENSP00000468611.1:n.1174G=
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|
ENST00000611848.1:c.840G=
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|
|
NM_005359.5:c.1527G= , LRG_318t1:c.1527G=
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NP_005350.1:p.Trp509=
|
|
NM_005359.6:c.1527G=
MANE Select
|
NP_005350.1:p.Trp509=
|
|