ENST00000379370.7:c.4914T>G
MANE Select
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ENSP00000368678.2:p.Ala1638=
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ENST00000651234.1:c.4599T>G
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ENSP00000499046.1:p.Ala1533=
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ENST00000652369.1:c.4599T>G
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ENSP00000498543.1:p.Ala1533=
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ENST00000379370.6:c.4914T>G
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ENSP00000368678.2:p.Ala1638=
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ENST00000620552.4:c.4500T>G
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ENSP00000484607.1:p.Ala1500=
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NM_001305275.1:c.4914T>G
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NP_001292204.1:p.Ala1638=
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NM_198576.3:c.4914T>G
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NP_940978.2:p.Ala1638=
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XM_005244749.2:c.4914T>G
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XP_005244806.1:p.Ala1638=
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XM_006710635.2:c.4914T>G
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XP_006710698.1:p.Ala1638=
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XM_011541429.1:c.4914T>G
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XP_011539731.1:p.Ala1638=
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XM_011541430.1:c.4041T>G
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XP_011539732.1:p.Ala1347=
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XM_011541431.1:c.3180T>G
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XP_011539733.1:p.Ala1060=
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XR_946650.1:n.4981T>G
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NM_001364727.1:c.4599T>G
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NP_001351656.1:p.Ala1533=
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XM_005244749.3:c.4914T>G
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XP_005244806.1:p.Ala1638=
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XM_011541429.2:c.4914T>G
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XP_011539731.1:p.Ala1638=
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XR_946650.2:n.4985T>G
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NM_001305275.2:c.4914T>G
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NP_001292204.1:p.Ala1638=
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NM_198576.4:c.4914T>G
MANE Select
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NP_940978.2:p.Ala1638=
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NM_001364727.2:c.4599T>G
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NP_001351656.1:p.Ala1533=
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