ENST00000269980.7:c.990C>G
MANE Select
|
ENSP00000269980.2:p.Thr330=
|
|
ENST00000269980.6:c.990C>G
|
ENSP00000269980.2:p.Thr330=
|
|
ENST00000457836.6:c.924C>G
|
ENSP00000416000.2:p.Thr308=
|
|
ENST00000540732.3:c.1092C>G
|
ENSP00000443246.1:p.Thr364=
|
|
ENST00000542943.5:c.903C>G
|
ENSP00000440345.1:p.Thr301=
|
|
ENST00000595085.5:c.922+68C>G
|
ENSP00000471150.2:n.922+68C>G
|
|
NM_000709.3:c.990C>G
|
NP_000700.1:p.Thr330=
|
|
NM_001164783.1:c.987C>G
|
NP_001158255.1:p.Thr329=
|
|
NM_000709.4:c.990C>G
MANE Select
|
NP_000700.1:p.Thr330=
|
|
NM_001164783.2:c.987C>G
|
NP_001158255.1:p.Thr329=
|
|