ENST00000237172.12:c.837A>G
MANE Select
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ENSP00000237172.7:p.Glu279=
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ENST00000237172.11:c.837A>G
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ENSP00000237172.7:p.Glu279=
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ENST00000370020.1:c.540A>G
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ENSP00000359037.1:p.Glu180=
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ENST00000393004.6:c.837A>G
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ENSP00000376728.1:p.Glu279=
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ENST00000498523.1:n.356A>G
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|
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NM_001289987.1:c.846A>G
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NP_001276916.1:p.Glu282=
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NM_001300866.1:c.837A>G
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NP_001287795.1:p.Glu279=
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|
NM_015687.3:c.837A>G
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NP_056502.1:p.Glu279=
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XM_005248713.2:c.837A>G
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XP_005248770.1:p.Glu279=
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XM_005248715.3:c.837A>G
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XP_005248772.1:p.Glu279=
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XM_011535756.1:c.93A>G
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XP_011534058.1:p.Glu31=
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NM_001289987.2:c.846A>G
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NP_001276916.1:p.Glu282=
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|
NM_001300866.2:c.837A>G
|
NP_001287795.1:p.Glu279=
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|
NM_015687.4:c.837A>G
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NP_056502.1:p.Glu279=
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|
XM_005248713.4:c.837A>G
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XP_005248770.1:p.Glu279=
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|
XM_005248715.5:c.837A>G
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XP_005248772.1:p.Glu279=
|
|
XM_011535756.2:c.93A>G
|
XP_011534058.1:p.Glu31=
|
|
NM_015687.5:c.837A>G
MANE Select
|
NP_056502.1:p.Glu279=
|
|
NM_001289987.3:c.846A>G
|
NP_001276916.1:p.Glu282=
|
|
NM_001300866.3:c.837A>G
|
NP_001287795.1:p.Glu279=
|
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