ENST00000269980.7:c.1217A>C
MANE Select
|
ENSP00000269980.2:p.Asn406Thr
|
|
ENST00000269980.6:c.1217A>C
|
ENSP00000269980.2:p.Asn406Thr
|
|
ENST00000457836.6:c.1226A>C
|
ENSP00000416000.2:p.Asn409Thr
|
|
ENST00000540732.3:c.1319A>C
|
ENSP00000443246.1:p.Asn440Thr
|
|
ENST00000544905.1:c.62-15A>C
|
|
|
ENST00000595085.5:c.922+1790A>C
|
ENSP00000471150.2:n.922+1790A>C
|
|
NM_000709.3:c.1217A>C
|
NP_000700.1:p.Asn406Thr
|
|
NM_001164783.1:c.1214A>C
|
NP_001158255.1:p.Asn405Thr
|
|
NM_000709.4:c.1217A>C
MANE Select
|
NP_000700.1:p.Asn406Thr
|
|
NM_001164783.2:c.1214A>C
|
NP_001158255.1:p.Asn405Thr
|
|