ENST00000449291.7:c.1586T>G
MANE Select
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ENSP00000401508.2:p.Val529Gly
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ENST00000340490.7:c.1671T>G
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ENSP00000341136.3:p.Gly557=
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ENST00000426292.7:c.1547T>G
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ENSP00000390949.3:p.Val516Gly
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ENST00000435154.7:c.*295T>G
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ENSP00000405670.3:n.*295T>G
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ENST00000449291.6:c.1586T>G
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ENSP00000401508.2:p.Val529Gly
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ENST00000460623.5:c.610T>G
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ENST00000464332.5:n.1130T>G
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ENST00000498076.5:n.365T>G
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ENST00000529179.1:n.370T>G
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NM_001286829.1:c.1547T>G
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NP_001273758.1:p.Val516Gly
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NM_145201.5:c.1586T>G
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NP_660202.3:p.Val529Gly
|
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XM_011517377.1:c.1323T>G
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XP_011515679.1:p.Gly441=
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NM_001363145.1:c.1505T>G
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NP_001350074.1:p.Val502Gly
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NM_001363146.1:c.902T>G
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NP_001350075.1:p.Val301Gly
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XM_017013975.2:c.1890T>G
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XP_016869464.1:p.Gly630=
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XM_017013976.2:c.1805T>G
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XP_016869465.1:p.Val602Gly
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XM_017013977.2:c.1590T>G
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XP_016869466.1:p.Gly530=
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XM_017013978.2:c.1542T>G
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XP_016869467.1:p.Gly514=
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XM_017013979.2:c.987T>G
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XP_016869468.1:p.Gly329=
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XM_024447332.1:c.960T>G
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XP_024303100.1:p.Gly320=
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XM_024447333.1:c.906T>G
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XP_024303101.1:p.Gly302=
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NM_145201.6:c.1586T>G
MANE Select
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NP_660202.3:p.Val529Gly
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NM_001286829.2:c.1547T>G
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NP_001273758.1:p.Val516Gly
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