ENST00000367698.4:c.1267G=
MANE Select
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ENSP00000356671.3:p.Ala423=
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ENST00000367698.3:c.1267G=
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ENSP00000356671.3:p.Ala423=
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ENST00000617423.4:c.652G=
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ENSP00000478688.1:p.Ala218=
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NM_000488.3:c.1267G= , LRG_577t1:c.1267G=
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NP_000479.1:p.Ala423=
|
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XM_005245198.2:c.1123G=
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XP_005245255.1:p.Ala375=
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NM_001365052.1:c.1123G=
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NP_001351981.1:p.Ala375=
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NM_000488.4:c.1267G=
MANE Select
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NP_000479.1:p.Ala423=
|
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NM_001365052.2:c.1123G=
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NP_001351981.1:p.Ala375=
|
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NM_001386302.1:c.1390G=
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NP_001373231.1:p.Ala464=
|
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NM_001386303.1:c.1348G=
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NP_001373232.1:p.Ala450=
|
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NM_001386304.1:c.1246G=
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NP_001373233.1:p.Ala416=
|
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NM_001386305.1:c.1210G=
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NP_001373234.1:p.Ala404=
|
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NM_001386306.1:c.1051G=
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NP_001373235.1:p.Ala351=
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