ENST00000269980.7:c.757G=
MANE Select
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ENSP00000269980.2:p.Ala253=
|
|
ENST00000269980.6:c.757G=
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ENSP00000269980.2:p.Ala253=
|
|
ENST00000457836.6:c.691G=
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ENSP00000416000.2:p.Ala231=
|
|
ENST00000535632.5:n.386G=
|
|
|
ENST00000540732.3:c.859G=
|
ENSP00000443246.1:p.Ala287=
|
|
ENST00000542943.5:c.670G=
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ENSP00000440345.1:p.Ala224=
|
|
ENST00000545787.1:n.385G=
|
|
|
ENST00000595085.5:c.757G=
|
ENSP00000471150.2:p.Ala253=
|
|
NM_000709.3:c.757G=
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NP_000700.1:p.Ala253=
|
|
NM_001164783.1:c.757G=
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NP_001158255.1:p.Ala253=
|
|
NM_000709.4:c.757G=
MANE Select
|
NP_000700.1:p.Ala253=
|
|
NM_001164783.2:c.757G=
|
NP_001158255.1:p.Ala253=
|
|