ENST00000269980.7:c.696C>G
MANE Select
|
ENSP00000269980.2:p.Val232=
|
|
ENST00000269980.6:c.696C>G
|
ENSP00000269980.2:p.Val232=
|
|
ENST00000457836.6:c.630C>G
|
ENSP00000416000.2:p.Val210=
|
|
ENST00000535632.5:n.325C>G
|
|
|
ENST00000540732.3:c.798C>G
|
ENSP00000443246.1:p.Val266=
|
|
ENST00000541315.1:c.596C>G
|
|
|
ENST00000542943.5:c.609C>G
|
ENSP00000440345.1:p.Val203=
|
|
ENST00000545787.1:n.324C>G
|
|
|
ENST00000595085.5:c.696C>G
|
ENSP00000471150.2:p.Val232=
|
|
NM_000709.3:c.696C>G
|
NP_000700.1:p.Val232=
|
|
NM_001164783.1:c.696C>G
|
NP_001158255.1:p.Val232=
|
|
NM_000709.4:c.696C>G
MANE Select
|
NP_000700.1:p.Val232=
|
|
NM_001164783.2:c.696C>G
|
NP_001158255.1:p.Val232=
|
|