ENST00000269980.7:c.118A>C
MANE Select
|
ENSP00000269980.2:p.Arg40=
|
|
ENST00000269980.6:c.118A>C
|
ENSP00000269980.2:p.Arg40=
|
|
ENST00000457836.6:c.58-6A>C
|
ENSP00000416000.2:n.58-6A>C
|
|
ENST00000538423.5:n.138A>C
|
|
|
ENST00000540732.3:c.220A>C
|
ENSP00000443246.1:p.Arg74=
|
|
ENST00000542943.5:c.118A>C
|
ENSP00000440345.1:p.Arg40=
|
|
ENST00000595085.5:c.118A>C
|
ENSP00000471150.2:p.Arg40=
|
|
ENST00000604424.1:n.360A>C
|
|
|
NM_000709.3:c.118A>C
|
NP_000700.1:p.Arg40=
|
|
NM_001164783.1:c.118A>C
|
NP_001158255.1:p.Arg40=
|
|
NM_000709.4:c.118A>C
MANE Select
|
NP_000700.1:p.Arg40=
|
|
NM_001164783.2:c.118A>C
|
NP_001158255.1:p.Arg40=
|
|