ENST00000449291.7:c.1589A>G
MANE Select
|
ENSP00000401508.2:p.Asn530Ser
|
|
ENST00000340490.7:c.1674A>G
|
ENSP00000341136.3:p.Glu558=
|
|
ENST00000426292.7:c.1550A>G
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ENSP00000390949.3:p.Asn517Ser
|
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ENST00000435154.7:c.*298A>G
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ENSP00000405670.3:n.*298A>G
|
|
ENST00000449291.6:c.1589A>G
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ENSP00000401508.2:p.Asn530Ser
|
|
ENST00000460623.5:c.613A>G
|
|
|
ENST00000464332.5:n.1133A>G
|
|
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ENST00000498076.5:n.368A>G
|
|
|
ENST00000529179.1:n.373A>G
|
|
|
NM_001286829.1:c.1550A>G
|
NP_001273758.1:p.Asn517Ser
|
|
NM_145201.5:c.1589A>G
|
NP_660202.3:p.Asn530Ser
|
|
XM_011517377.1:c.1326A>G
|
XP_011515679.1:p.Glu442=
|
|
NM_001363145.1:c.1508A>G
|
NP_001350074.1:p.Asn503Ser
|
|
NM_001363146.1:c.905A>G
|
NP_001350075.1:p.Asn302Ser
|
|
XM_017013975.2:c.1893A>G
|
XP_016869464.1:p.Glu631=
|
|
XM_017013976.2:c.1808A>G
|
XP_016869465.1:p.Asn603Ser
|
|
XM_017013977.2:c.1593A>G
|
XP_016869466.1:p.Glu531=
|
|
XM_017013978.2:c.1545A>G
|
XP_016869467.1:p.Glu515=
|
|
XM_017013979.2:c.990A>G
|
XP_016869468.1:p.Glu330=
|
|
XM_024447332.1:c.963A>G
|
XP_024303100.1:p.Glu321=
|
|
XM_024447333.1:c.909A>G
|
XP_024303101.1:p.Glu303=
|
|
NM_145201.6:c.1589A>G
MANE Select
|
NP_660202.3:p.Asn530Ser
|
|
NM_001286829.2:c.1550A>G
|
NP_001273758.1:p.Asn517Ser
|
|