ENST00000269980.7:c.795G>T
MANE Select
|
ENSP00000269980.2:p.Arg265=
|
|
ENST00000269980.6:c.795G>T
|
ENSP00000269980.2:p.Arg265=
|
|
ENST00000457836.6:c.729G>T
|
ENSP00000416000.2:p.Arg243=
|
|
ENST00000535632.5:n.424G>T
|
|
|
ENST00000540732.3:c.897G>T
|
ENSP00000443246.1:p.Arg299=
|
|
ENST00000542943.5:c.708G>T
|
ENSP00000440345.1:p.Arg236=
|
|
ENST00000545787.1:n.423G>T
|
|
|
ENST00000595085.5:c.795G>T
|
ENSP00000471150.2:p.Arg265=
|
|
NM_000709.3:c.795G>T
|
NP_000700.1:p.Arg265=
|
|
NM_001164783.1:c.795G>T
|
NP_001158255.1:p.Arg265=
|
|
NM_000709.4:c.795G>T
MANE Select
|
NP_000700.1:p.Arg265=
|
|
NM_001164783.2:c.795G>T
|
NP_001158255.1:p.Arg265=
|
|