ENST00000269980.7:c.351C>A
MANE Select
|
ENSP00000269980.2:p.Arg117=
|
|
ENST00000269980.6:c.351C>A
|
ENSP00000269980.2:p.Arg117=
|
|
ENST00000457836.6:c.285C>A
|
ENSP00000416000.2:p.Arg95=
|
|
ENST00000538423.5:n.477C>A
|
|
|
ENST00000540732.3:c.453C>A
|
ENSP00000443246.1:p.Arg151=
|
|
ENST00000541315.1:c.158C>A
|
|
|
ENST00000542943.5:c.288+169C>A
|
ENSP00000440345.1:n.288+169C>A
|
|
ENST00000595085.5:c.351C>A
|
ENSP00000471150.2:p.Arg117=
|
|
NM_000709.3:c.351C>A
|
NP_000700.1:p.Arg117=
|
|
NM_001164783.1:c.351C>A
|
NP_001158255.1:p.Arg117=
|
|
NM_000709.4:c.351C>A
MANE Select
|
NP_000700.1:p.Arg117=
|
|
NM_001164783.2:c.351C>A
|
NP_001158255.1:p.Arg117=
|
|