ENST00000269980.7:c.669C>T
MANE Select
|
ENSP00000269980.2:p.Ala223=
|
|
ENST00000269980.6:c.669C>T
|
ENSP00000269980.2:p.Ala223=
|
|
ENST00000457836.6:c.603C>T
|
ENSP00000416000.2:p.Ala201=
|
|
ENST00000535632.5:n.298C>T
|
|
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ENST00000538423.5:n.795C>T
|
|
|
ENST00000540732.3:c.771C>T
|
ENSP00000443246.1:p.Ala257=
|
|
ENST00000541315.1:c.569C>T
|
|
|
ENST00000542943.5:c.582C>T
|
ENSP00000440345.1:p.Ala194=
|
|
ENST00000545787.1:n.297C>T
|
|
|
ENST00000595085.5:c.669C>T
|
ENSP00000471150.2:p.Ala223=
|
|
NM_000709.3:c.669C>T
|
NP_000700.1:p.Ala223=
|
|
NM_001164783.1:c.669C>T
|
NP_001158255.1:p.Ala223=
|
|
NM_000709.4:c.669C>T
MANE Select
|
NP_000700.1:p.Ala223=
|
|
NM_001164783.2:c.669C>T
|
NP_001158255.1:p.Ala223=
|
|