ENST00000367698.4:c.1247C>A
MANE Select
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ENSP00000356671.3:p.Ala416Glu
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ENST00000367698.3:c.1247C>A
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ENSP00000356671.3:p.Ala416Glu
|
|
ENST00000617423.4:c.632C>A
|
ENSP00000478688.1:p.Ala211Glu
|
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NM_000488.3:c.1247C>A , LRG_577t1:c.1247C>A
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NP_000479.1:p.Ala416Glu
|
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XM_005245198.2:c.1103C>A
|
XP_005245255.1:p.Ala368Glu
|
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NM_001365052.1:c.1103C>A
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NP_001351981.1:p.Ala368Glu
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NM_000488.4:c.1247C>A
MANE Select
|
NP_000479.1:p.Ala416Glu
|
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NM_001365052.2:c.1103C>A
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NP_001351981.1:p.Ala368Glu
|
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NM_001386302.1:c.1370C>A
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NP_001373231.1:p.Ala457Glu
|
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NM_001386303.1:c.1328C>A
|
NP_001373232.1:p.Ala443Glu
|
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NM_001386304.1:c.1226C>A
|
NP_001373233.1:p.Ala409Glu
|
|
NM_001386305.1:c.1190C>A
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NP_001373234.1:p.Ala397Glu
|
|
NM_001386306.1:c.1031C>A
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NP_001373235.1:p.Ala344Glu
|
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