ENST00000477226.6:n.220A>T
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|
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ENST00000683013.1:n.134A>T
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|
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ENST00000373960.4:c.746A>T
MANE Select
|
ENSP00000363071.3:p.Glu249Val
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ENST00000373960.3:c.746A>T
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ENSP00000363071.3:p.Glu249Val
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ENST00000477226.5:n.218A>T
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|
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ENST00000492726.1:n.141A>T
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NM_001927.3:c.746A>T , LRG_380t1:c.746A>T
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NP_001918.3:p.Glu249Val
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|
NM_001927.4:c.746A>T
MANE Select
|
NP_001918.3:p.Glu249Val
|
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NM_001382708.1:c.743A>T
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NP_001369637.1:p.Glu248Val
|
|
NM_001382709.1:c.735+159A>T
|
NP_001369638.1:n.735+159A>T
|
|
NM_001382710.1:c.746A>T
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NP_001369639.1:p.Glu249Val
|
|
NM_001382711.1:c.746A>T
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NP_001369640.1:p.Glu249Val
|
|
NM_001382712.1:c.746A>T
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NP_001369641.1:p.Glu249Val
|
|
NM_001382713.1:c.496-20A>T
|
NP_001369642.1:n.496-20A>T
|
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