ENST00000302068.9:c.1146C=
MANE Select
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ENSP00000306099.4:p.Ala382=
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ENST00000302068.8:c.1146C=
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ENSP00000306099.4:p.Ala382=
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ENST00000502545.5:n.939+394C=
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ENST00000509493.1:c.489C=
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ENSP00000426757.1:p.Ala163=
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NM_001184741.1:c.969C=
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NP_001171670.1:p.Ala323=
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NM_005141.4:c.1146C= , LRG_558t1:c.1146C=
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NP_005132.2:p.Ala382=
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NM_001382759.1:c.1014C=
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NP_001369688.1:p.Ala338=
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NM_001382760.1:c.1146C=
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NP_001369689.1:p.Ala382=
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NM_001382761.1:c.1146C=
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NP_001369690.1:p.Ala382=
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NM_001382762.1:c.846C=
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NP_001369691.1:p.Ala282=
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NM_001382763.1:c.1137C=
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NP_001369692.1:p.Ala379=
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NM_001382764.1:c.1080+66C=
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NP_001369693.1:n.1080+66C=
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NM_001382765.1:c.1146C=
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NP_001369694.1:p.Ala382=
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NM_005141.5:c.1146C=
MANE Select
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NP_005132.2:p.Ala382=
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