ENST00000449291.7:c.1571G>A
MANE Select
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ENSP00000401508.2:p.Arg524Lys
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ENST00000340490.7:c.1656G>A
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ENSP00000341136.3:p.Glu552=
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ENST00000426292.7:c.1532G>A
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ENSP00000390949.3:p.Arg511Lys
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ENST00000435154.7:c.*280G>A
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ENSP00000405670.3:n.*280G>A
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ENST00000449291.6:c.1571G>A
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ENSP00000401508.2:p.Arg524Lys
|
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ENST00000460623.5:c.595G>A
|
|
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ENST00000464332.5:n.1115G>A
|
|
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ENST00000498076.5:n.350G>A
|
|
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ENST00000529179.1:n.355G>A
|
|
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NM_001286829.1:c.1532G>A
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NP_001273758.1:p.Arg511Lys
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NM_145201.5:c.1571G>A
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NP_660202.3:p.Arg524Lys
|
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XM_011517377.1:c.1308G>A
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XP_011515679.1:p.Glu436=
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NM_001363145.1:c.1490G>A
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NP_001350074.1:p.Arg497Lys
|
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NM_001363146.1:c.887G>A
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NP_001350075.1:p.Arg296Lys
|
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XM_017013975.2:c.1875G>A
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XP_016869464.1:p.Glu625=
|
|
XM_017013976.2:c.1790G>A
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XP_016869465.1:p.Arg597Lys
|
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XM_017013977.2:c.1575G>A
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XP_016869466.1:p.Glu525=
|
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XM_017013978.2:c.1527G>A
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XP_016869467.1:p.Glu509=
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XM_017013979.2:c.972G>A
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XP_016869468.1:p.Glu324=
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XM_024447332.1:c.945G>A
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XP_024303100.1:p.Glu315=
|
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XM_024447333.1:c.891G>A
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XP_024303101.1:p.Glu297=
|
|
NM_145201.6:c.1571G>A
MANE Select
|
NP_660202.3:p.Arg524Lys
|
|
NM_001286829.2:c.1532G>A
|
NP_001273758.1:p.Arg511Lys
|
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