ENST00000449291.7:c.1573C>G
MANE Select
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ENSP00000401508.2:p.Leu525Val
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ENST00000340490.7:c.1658C>G
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ENSP00000341136.3:p.Ala553Gly
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ENST00000426292.7:c.1534C>G
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ENSP00000390949.3:p.Leu512Val
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ENST00000435154.7:c.*282C>G
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ENSP00000405670.3:n.*282C>G
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ENST00000449291.6:c.1573C>G
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ENSP00000401508.2:p.Leu525Val
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ENST00000460623.5:c.597C>G
|
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ENST00000464332.5:n.1117C>G
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ENST00000498076.5:n.352C>G
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ENST00000529179.1:n.357C>G
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NM_001286829.1:c.1534C>G
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NP_001273758.1:p.Leu512Val
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NM_145201.5:c.1573C>G
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NP_660202.3:p.Leu525Val
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XM_011517377.1:c.1310C>G
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XP_011515679.1:p.Ala437Gly
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NM_001363145.1:c.1492C>G
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NP_001350074.1:p.Leu498Val
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NM_001363146.1:c.889C>G
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NP_001350075.1:p.Leu297Val
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XM_017013975.2:c.1877C>G
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XP_016869464.1:p.Ala626Gly
|
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XM_017013976.2:c.1792C>G
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XP_016869465.1:p.Leu598Val
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XM_017013977.2:c.1577C>G
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XP_016869466.1:p.Ala526Gly
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XM_017013978.2:c.1529C>G
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XP_016869467.1:p.Ala510Gly
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XM_017013979.2:c.974C>G
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XP_016869468.1:p.Ala325Gly
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XM_024447332.1:c.947C>G
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XP_024303100.1:p.Ala316Gly
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XM_024447333.1:c.893C>G
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XP_024303101.1:p.Ala298Gly
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NM_145201.6:c.1573C>G
MANE Select
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NP_660202.3:p.Leu525Val
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NM_001286829.2:c.1534C>G
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NP_001273758.1:p.Leu512Val
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