ENST00000593677.2:c.1836A>C
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ENST00000688602.1:c.3233A>C
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ENST00000689936.1:c.3205A>C
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ENST00000692547.1:n.293A>C
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ENST00000359596.8:c.14900A>C
MANE Select
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ENSP00000352608.2:p.Asp4967Ala
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ENST00000355481.8:c.14885A>C
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ENSP00000347667.3:p.Asp4962Ala
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ENST00000359596.7:c.14900A>C
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ENSP00000352608.2:p.Asp4967Ala
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ENST00000360985.7:c.14882A>C
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ENSP00000354254.4:p.Asp4961Ala
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NM_000540.2:c.14900A>C , LRG_766t1:c.14900A>C
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NP_000531.2:p.Asp4967Ala
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NM_001042723.1:c.14885A>C
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NP_001036188.1:p.Asp4962Ala
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XM_006723317.1:c.14882A>C
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XP_006723380.1:p.Asp4961Ala
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XM_006723319.1:c.14867A>C
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XP_006723382.1:p.Asp4956Ala
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XM_011527204.1:c.14897A>C
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XP_011525506.1:p.Asp4966Ala
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XM_011527205.1:c.14813A>C
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XP_011525507.1:p.Asp4938Ala
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XM_006723317.2:c.14882A>C
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XP_006723380.1:p.Asp4961Ala
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XM_006723319.2:c.14867A>C
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XP_006723382.1:p.Asp4956Ala
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XM_011527205.2:c.14813A>C
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XP_011525507.1:p.Asp4938Ala
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NM_000540.3:c.14900A>C
MANE Select
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NP_000531.2:p.Asp4967Ala
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NM_001042723.2:c.14885A>C
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NP_001036188.1:p.Asp4962Ala
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