ENST00000269980.7:c.156C>G
MANE Select
|
ENSP00000269980.2:p.Pro52=
|
|
ENST00000269980.6:c.156C>G
|
ENSP00000269980.2:p.Pro52=
|
|
ENST00000457836.6:c.90C>G
|
ENSP00000416000.2:p.Pro30=
|
|
ENST00000538423.5:n.176C>G
|
|
|
ENST00000540732.3:c.258C>G
|
ENSP00000443246.1:p.Pro86=
|
|
ENST00000542943.5:c.156C>G
|
ENSP00000440345.1:p.Pro52=
|
|
ENST00000595085.5:c.156C>G
|
ENSP00000471150.2:p.Pro52=
|
|
ENST00000604424.1:n.398C>G
|
|
|
NM_000709.3:c.156C>G
|
NP_000700.1:p.Pro52=
|
|
NM_001164783.1:c.156C>G
|
NP_001158255.1:p.Pro52=
|
|
NM_000709.4:c.156C>G
MANE Select
|
NP_000700.1:p.Pro52=
|
|
NM_001164783.2:c.156C>G
|
NP_001158255.1:p.Pro52=
|
|