ENST00000449291.7:c.1491C>T
MANE Select
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ENSP00000401508.2:p.Ala497=
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ENST00000340490.7:c.1491C>T
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ENSP00000341136.3:p.Ala497=
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ENST00000426292.7:c.1452C>T
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ENSP00000390949.3:p.Ala484=
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ENST00000435154.7:c.*115C>T
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ENSP00000405670.3:n.*115C>T
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ENST00000449291.6:c.1491C>T
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ENSP00000401508.2:p.Ala497=
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ENST00000460623.5:c.430C>T
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ENST00000464332.5:n.1035C>T
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ENST00000498076.5:n.270C>T
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ENST00000529179.1:n.275C>T
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NM_001286829.1:c.1452C>T
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NP_001273758.1:p.Ala484=
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NM_145201.5:c.1491C>T
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NP_660202.3:p.Ala497=
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XM_011517377.1:c.1292-149C>T
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XP_011515679.1:n.1292-149C>T
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NM_001363145.1:c.1410C>T
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NP_001350074.1:p.Ala470=
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NM_001363146.1:c.807C>T
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NP_001350075.1:p.Ala269=
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XM_017013975.2:c.1710C>T
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XP_016869464.1:p.Ala570=
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XM_017013976.2:c.1710C>T
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XP_016869465.1:p.Ala570=
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XM_017013977.2:c.1410C>T
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XP_016869466.1:p.Ala470=
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XM_017013978.2:c.1511-149C>T
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XP_016869467.1:n.1511-149C>T
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XM_017013979.2:c.807C>T
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XP_016869468.1:p.Ala269=
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XM_024447332.1:c.929-149C>T
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XP_024303100.1:n.929-149C>T
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XM_024447333.1:c.726C>T
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XP_024303101.1:p.Ala242=
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NM_145201.6:c.1491C>T
MANE Select
|
NP_660202.3:p.Ala497=
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NM_001286829.2:c.1452C>T
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NP_001273758.1:p.Ala484=
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