ENST00000449291.7:c.1555G>A
MANE Select
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ENSP00000401508.2:p.Val519Met
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ENST00000340490.7:c.1640G>A
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ENSP00000341136.3:p.Gly547Asp
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|
ENST00000426292.7:c.1516G>A
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ENSP00000390949.3:p.Val506Met
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ENST00000435154.7:c.*264G>A
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ENSP00000405670.3:n.*264G>A
|
|
ENST00000449291.6:c.1555G>A
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ENSP00000401508.2:p.Val519Met
|
|
ENST00000460623.5:c.579G>A
|
|
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ENST00000464332.5:n.1099G>A
|
|
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ENST00000498076.5:n.334G>A
|
|
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ENST00000529179.1:n.339G>A
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|
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NM_001286829.1:c.1516G>A
|
NP_001273758.1:p.Val506Met
|
|
NM_145201.5:c.1555G>A
|
NP_660202.3:p.Val519Met
|
|
XM_011517377.1:c.1292G>A
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XP_011515679.1:p.Gly431Asp
|
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NM_001363145.1:c.1474G>A
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NP_001350074.1:p.Val492Met
|
|
NM_001363146.1:c.871G>A
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NP_001350075.1:p.Val291Met
|
|
XM_017013975.2:c.1859G>A
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XP_016869464.1:p.Gly620Asp
|
|
XM_017013976.2:c.1774G>A
|
XP_016869465.1:p.Val592Met
|
|
XM_017013977.2:c.1559G>A
|
XP_016869466.1:p.Gly520Asp
|
|
XM_017013978.2:c.1511G>A
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XP_016869467.1:p.Gly504Asp
|
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XM_017013979.2:c.956G>A
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XP_016869468.1:p.Gly319Asp
|
|
XM_024447332.1:c.929G>A
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XP_024303100.1:p.Gly310Asp
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XM_024447333.1:c.875G>A
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XP_024303101.1:p.Gly292Asp
|
|
NM_145201.6:c.1555G>A
MANE Select
|
NP_660202.3:p.Val519Met
|
|
NM_001286829.2:c.1516G>A
|
NP_001273758.1:p.Val506Met
|
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