ENST00000269980.7:c.894G>C
MANE Select
|
ENSP00000269980.2:p.Val298=
|
|
ENST00000269980.6:c.894G>C
|
ENSP00000269980.2:p.Val298=
|
|
ENST00000457836.6:c.828G>C
|
ENSP00000416000.2:p.Val276=
|
|
ENST00000535632.5:n.523G>C
|
|
|
ENST00000540732.3:c.996G>C
|
ENSP00000443246.1:p.Val332=
|
|
ENST00000542943.5:c.807G>C
|
ENSP00000440345.1:p.Val269=
|
|
ENST00000545787.1:n.522G>C
|
|
|
ENST00000595085.5:c.894G>C
|
ENSP00000471150.2:p.Val298=
|
|
NM_000709.3:c.894G>C
|
NP_000700.1:p.Val298=
|
|
NM_001164783.1:c.891G>C
|
NP_001158255.1:p.Val297=
|
|
NM_000709.4:c.894G>C
MANE Select
|
NP_000700.1:p.Val298=
|
|
NM_001164783.2:c.891G>C
|
NP_001158255.1:p.Val297=
|
|