ENST00000269980.7:c.996G=
MANE Select
|
ENSP00000269980.2:p.Arg332=
|
|
ENST00000269980.6:c.996G=
|
ENSP00000269980.2:p.Arg332=
|
|
ENST00000457836.6:c.1005G=
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ENSP00000416000.2:p.Arg335=
|
|
ENST00000540732.3:c.1098G=
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ENSP00000443246.1:p.Arg366=
|
|
ENST00000542943.5:c.909G=
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ENSP00000440345.1:p.Arg303=
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|
ENST00000595085.5:c.922+301G=
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ENSP00000471150.2:n.922+301G=
|
|
NM_000709.3:c.996G=
|
NP_000700.1:p.Arg332=
|
|
NM_001164783.1:c.993G=
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NP_001158255.1:p.Arg331=
|
|
NM_000709.4:c.996G=
MANE Select
|
NP_000700.1:p.Arg332=
|
|
NM_001164783.2:c.993G=
|
NP_001158255.1:p.Arg331=
|
|