ENST00000449291.7:c.1585G>A
MANE Select
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ENSP00000401508.2:p.Val529Met
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ENST00000340490.7:c.1670G>A
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ENSP00000341136.3:p.Gly557Asp
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|
ENST00000426292.7:c.1546G>A
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ENSP00000390949.3:p.Val516Met
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ENST00000435154.7:c.*294G>A
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ENSP00000405670.3:n.*294G>A
|
|
ENST00000449291.6:c.1585G>A
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ENSP00000401508.2:p.Val529Met
|
|
ENST00000460623.5:c.609G>A
|
|
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ENST00000464332.5:n.1129G>A
|
|
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ENST00000498076.5:n.364G>A
|
|
|
ENST00000529179.1:n.369G>A
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|
|
NM_001286829.1:c.1546G>A
|
NP_001273758.1:p.Val516Met
|
|
NM_145201.5:c.1585G>A
|
NP_660202.3:p.Val529Met
|
|
XM_011517377.1:c.1322G>A
|
XP_011515679.1:p.Gly441Asp
|
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NM_001363145.1:c.1504G>A
|
NP_001350074.1:p.Val502Met
|
|
NM_001363146.1:c.901G>A
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NP_001350075.1:p.Val301Met
|
|
XM_017013975.2:c.1889G>A
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XP_016869464.1:p.Gly630Asp
|
|
XM_017013976.2:c.1804G>A
|
XP_016869465.1:p.Val602Met
|
|
XM_017013977.2:c.1589G>A
|
XP_016869466.1:p.Gly530Asp
|
|
XM_017013978.2:c.1541G>A
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XP_016869467.1:p.Gly514Asp
|
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XM_017013979.2:c.986G>A
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XP_016869468.1:p.Gly329Asp
|
|
XM_024447332.1:c.959G>A
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XP_024303100.1:p.Gly320Asp
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XM_024447333.1:c.905G>A
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XP_024303101.1:p.Gly302Asp
|
|
NM_145201.6:c.1585G>A
MANE Select
|
NP_660202.3:p.Val529Met
|
|
NM_001286829.2:c.1546G>A
|
NP_001273758.1:p.Val516Met
|
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