ENST00000269980.7:c.808G=
MANE Select
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ENSP00000269980.2:p.Ala270=
|
|
ENST00000269980.6:c.808G=
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ENSP00000269980.2:p.Ala270=
|
|
ENST00000457836.6:c.742G=
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ENSP00000416000.2:p.Ala248=
|
|
ENST00000535632.5:n.437G=
|
|
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ENST00000540732.3:c.910G=
|
ENSP00000443246.1:p.Ala304=
|
|
ENST00000542943.5:c.721G=
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ENSP00000440345.1:p.Ala241=
|
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ENST00000545787.1:n.436G=
|
|
|
ENST00000595085.5:c.808G=
|
ENSP00000471150.2:p.Ala270=
|
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NM_000709.3:c.808G=
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NP_000700.1:p.Ala270=
|
|
NM_001164783.1:c.808G=
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NP_001158255.1:p.Ala270=
|
|
NM_000709.4:c.808G=
MANE Select
|
NP_000700.1:p.Ala270=
|
|
NM_001164783.2:c.808G=
|
NP_001158255.1:p.Ala270=
|
|