ENST00000269980.7:c.1217A>G
MANE Select
|
ENSP00000269980.2:p.Asn406Ser
|
|
ENST00000269980.6:c.1217A>G
|
ENSP00000269980.2:p.Asn406Ser
|
|
ENST00000457836.6:c.1226A>G
|
ENSP00000416000.2:p.Asn409Ser
|
|
ENST00000540732.3:c.1319A>G
|
ENSP00000443246.1:p.Asn440Ser
|
|
ENST00000544905.1:c.62-15A>G
|
|
|
ENST00000595085.5:c.922+1790A>G
|
ENSP00000471150.2:n.922+1790A>G
|
|
NM_000709.3:c.1217A>G
|
NP_000700.1:p.Asn406Ser
|
|
NM_001164783.1:c.1214A>G
|
NP_001158255.1:p.Asn405Ser
|
|
NM_000709.4:c.1217A>G
MANE Select
|
NP_000700.1:p.Asn406Ser
|
|
NM_001164783.2:c.1214A>G
|
NP_001158255.1:p.Asn405Ser
|
|