ENST00000315491.12:c.1304A>C
MANE Select
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ENSP00000320295.7:p.Glu435Ala
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ENST00000680788.1:n.4725A>C
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|
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ENST00000315491.11:c.1304A>C
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ENSP00000320295.7:p.Glu435Ala
|
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ENST00000554444.5:c.1088A>C
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ENSP00000451617.1:p.Glu363Ala
|
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ENST00000555576.5:c.277+2177A>C
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ENSP00000452554.1:n.277+2177A>C
|
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ENST00000555609.5:c.*1389A>C
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ENSP00000451276.1:n.*1389A>C
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ENST00000556922.1:c.2345A>C
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ENSP00000451560.1:p.Glu782Ala
|
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NM_001197181.1:c.1088A>C
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NP_001184110.1:p.Glu363Ala
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NM_006086.3:c.1304A>C
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NP_006077.2:p.Glu435Ala
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NM_006086.4:c.1304A>C
MANE Select
|
NP_006077.2:p.Glu435Ala
|
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NM_001197181.2:c.1088A>C
|
NP_001184110.1:p.Glu363Ala
|
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