ENST00000449291.7:c.1581C>G
MANE Select
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ENSP00000401508.2:p.Ala527=
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ENST00000340490.7:c.1666C>G
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ENSP00000341136.3:p.Pro556Ala
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ENST00000426292.7:c.1542C>G
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ENSP00000390949.3:p.Ala514=
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ENST00000435154.7:c.*290C>G
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ENSP00000405670.3:n.*290C>G
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ENST00000449291.6:c.1581C>G
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ENSP00000401508.2:p.Ala527=
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ENST00000460623.5:c.605C>G
|
|
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ENST00000464332.5:n.1125C>G
|
|
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ENST00000498076.5:n.360C>G
|
|
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ENST00000529179.1:n.365C>G
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|
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NM_001286829.1:c.1542C>G
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NP_001273758.1:p.Ala514=
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NM_145201.5:c.1581C>G
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NP_660202.3:p.Ala527=
|
|
XM_011517377.1:c.1318C>G
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XP_011515679.1:p.Pro440Ala
|
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NM_001363145.1:c.1500C>G
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NP_001350074.1:p.Ala500=
|
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NM_001363146.1:c.897C>G
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NP_001350075.1:p.Ala299=
|
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XM_017013975.2:c.1885C>G
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XP_016869464.1:p.Pro629Ala
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XM_017013976.2:c.1800C>G
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XP_016869465.1:p.Ala600=
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XM_017013977.2:c.1585C>G
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XP_016869466.1:p.Pro529Ala
|
|
XM_017013978.2:c.1537C>G
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XP_016869467.1:p.Pro513Ala
|
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XM_017013979.2:c.982C>G
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XP_016869468.1:p.Pro328Ala
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XM_024447332.1:c.955C>G
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XP_024303100.1:p.Pro319Ala
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XM_024447333.1:c.901C>G
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XP_024303101.1:p.Pro301Ala
|
|
NM_145201.6:c.1581C>G
MANE Select
|
NP_660202.3:p.Ala527=
|
|
NM_001286829.2:c.1542C>G
|
NP_001273758.1:p.Ala514=
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