ENST00000269980.7:c.858A>C
MANE Select
|
ENSP00000269980.2:p.Ala286=
|
|
ENST00000269980.6:c.858A>C
|
ENSP00000269980.2:p.Ala286=
|
|
ENST00000457836.6:c.792A>C
|
ENSP00000416000.2:p.Ala264=
|
|
ENST00000535632.5:n.487A>C
|
|
|
ENST00000540732.3:c.960A>C
|
ENSP00000443246.1:p.Ala320=
|
|
ENST00000542943.5:c.771A>C
|
ENSP00000440345.1:p.Ala257=
|
|
ENST00000545787.1:n.486A>C
|
|
|
ENST00000595085.5:c.858A>C
|
ENSP00000471150.2:p.Ala286=
|
|
NM_000709.3:c.858A>C
|
NP_000700.1:p.Ala286=
|
|
NM_001164783.1:c.855A>C
|
NP_001158255.1:p.Ala285=
|
|
NM_000709.4:c.858A>C
MANE Select
|
NP_000700.1:p.Ala286=
|
|
NM_001164783.2:c.855A>C
|
NP_001158255.1:p.Ala285=
|
|