ENST00000262027.10:c.1414A>G
MANE Select
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ENSP00000262027.5:p.Ser472Gly
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ENST00000262027.9:c.1414A>G
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ENSP00000262027.5:p.Ser472Gly
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ENST00000447721.6:n.1056A>G
|
|
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ENST00000537638.6:c.1414A>G
|
ENSP00000446168.2:p.Ser472Gly
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ENST00000545888.6:c.*915A>G
|
ENSP00000439307.2:n.*915A>G
|
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ENST00000546971.5:n.158A>G
|
|
|
ENST00000548944.1:c.134-4752A>G
|
ENSP00000449071.1:n.134-4752A>G
|
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ENST00000549603.1:n.360A>G
|
|
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ENST00000628866.2:c.*915A>G
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ENSP00000486738.1:n.*915A>G
|
|
NM_004990.3:c.1414A>G
|
NP_004981.2:p.Ser472Gly
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XM_006719398.2:c.712A>G
|
XP_006719461.1:p.Ser238Gly
|
|
XM_011538353.1:c.1414A>G
|
XP_011536655.1:p.Ser472Gly
|
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XM_006719398.4:c.712A>G
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XP_006719461.1:p.Ser238Gly
|
|
XR_001748704.2:n.1437A>G
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|
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XR_002957327.1:n.1361A>G
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|
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NM_004990.4:c.1414A>G
MANE Select
|
NP_004981.2:p.Ser472Gly
|
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