ENST00000211998.10:c.804A=
MANE Select
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ENSP00000211998.5:p.Arg268=
|
|
ENST00000211998.8:c.804A=
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ENSP00000211998.4:p.Arg268=
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|
ENST00000372755.7:c.804A=
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ENSP00000361841.3:p.Arg268=
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|
ENST00000478896.2:n.332-18580A=
|
|
|
ENST00000623461.3:n.3607A=
|
|
|
ENST00000624354.3:c.*559A=
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ENSP00000485551.1:n.*559A=
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|
NM_003373.3:c.804A=
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NP_003364.1:p.Arg268=
|
|
NM_014000.2:c.804A= , LRG_383t1:c.804A=
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NP_054706.1:p.Arg268=
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|
XM_005270142.1:c.807A=
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XP_005270199.1:p.Arg269=
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|
XM_005270143.1:c.807A=
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XP_005270200.1:p.Arg269=
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|
XR_001747501.1:n.90-4747T=
|
|
|
NM_003373.4:c.804A=
|
NP_003364.1:p.Arg268=
|
|
NM_014000.3:c.804A=
MANE Select
|
NP_054706.1:p.Arg268=
|
|