ENST00000449291.7:c.1588A>G
MANE Select
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ENSP00000401508.2:p.Asn530Asp
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ENST00000340490.7:c.1673A>G
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ENSP00000341136.3:p.Glu558Gly
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ENST00000426292.7:c.1549A>G
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ENSP00000390949.3:p.Asn517Asp
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ENST00000435154.7:c.*297A>G
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ENSP00000405670.3:n.*297A>G
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ENST00000449291.6:c.1588A>G
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ENSP00000401508.2:p.Asn530Asp
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ENST00000460623.5:c.612A>G
|
|
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ENST00000464332.5:n.1132A>G
|
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ENST00000498076.5:n.367A>G
|
|
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ENST00000529179.1:n.372A>G
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NM_001286829.1:c.1549A>G
|
NP_001273758.1:p.Asn517Asp
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NM_145201.5:c.1588A>G
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NP_660202.3:p.Asn530Asp
|
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XM_011517377.1:c.1325A>G
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XP_011515679.1:p.Glu442Gly
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NM_001363145.1:c.1507A>G
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NP_001350074.1:p.Asn503Asp
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NM_001363146.1:c.904A>G
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NP_001350075.1:p.Asn302Asp
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XM_017013975.2:c.1892A>G
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XP_016869464.1:p.Glu631Gly
|
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XM_017013976.2:c.1807A>G
|
XP_016869465.1:p.Asn603Asp
|
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XM_017013977.2:c.1592A>G
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XP_016869466.1:p.Glu531Gly
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XM_017013978.2:c.1544A>G
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XP_016869467.1:p.Glu515Gly
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XM_017013979.2:c.989A>G
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XP_016869468.1:p.Glu330Gly
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XM_024447332.1:c.962A>G
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XP_024303100.1:p.Glu321Gly
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XM_024447333.1:c.908A>G
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XP_024303101.1:p.Glu303Gly
|
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NM_145201.6:c.1588A>G
MANE Select
|
NP_660202.3:p.Asn530Asp
|
|
NM_001286829.2:c.1549A>G
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NP_001273758.1:p.Asn517Asp
|
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