ENST00000269980.7:c.723C>A
MANE Select
|
ENSP00000269980.2:p.Ala241=
|
|
ENST00000269980.6:c.723C>A
|
ENSP00000269980.2:p.Ala241=
|
|
ENST00000457836.6:c.657C>A
|
ENSP00000416000.2:p.Ala219=
|
|
ENST00000535632.5:n.352C>A
|
|
|
ENST00000540732.3:c.825C>A
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ENSP00000443246.1:p.Ala275=
|
|
ENST00000541315.1:c.623C>A
|
|
|
ENST00000542943.5:c.636C>A
|
ENSP00000440345.1:p.Ala212=
|
|
ENST00000545787.1:n.351C>A
|
|
|
ENST00000595085.5:c.723C>A
|
ENSP00000471150.2:p.Ala241=
|
|
NM_000709.3:c.723C>A
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NP_000700.1:p.Ala241=
|
|
NM_001164783.1:c.723C>A
|
NP_001158255.1:p.Ala241=
|
|
NM_000709.4:c.723C>A
MANE Select
|
NP_000700.1:p.Ala241=
|
|
NM_001164783.2:c.723C>A
|
NP_001158255.1:p.Ala241=
|
|