ENST00000269980.7:c.1013C>A
MANE Select
|
ENSP00000269980.2:p.Thr338Asn
|
|
ENST00000269980.6:c.1013C>A
|
ENSP00000269980.2:p.Thr338Asn
|
|
ENST00000457836.6:c.1022C>A
|
ENSP00000416000.2:p.Thr341Asn
|
|
ENST00000540732.3:c.1115C>A
|
ENSP00000443246.1:p.Thr372Asn
|
|
ENST00000542943.5:c.926C>A
|
ENSP00000440345.1:p.Thr309Asn
|
|
ENST00000595085.5:c.922+318C>A
|
ENSP00000471150.2:n.922+318C>A
|
|
NM_000709.3:c.1013C>A
|
NP_000700.1:p.Thr338Asn
|
|
NM_001164783.1:c.1010C>A
|
NP_001158255.1:p.Thr337Asn
|
|
NM_000709.4:c.1013C>A
MANE Select
|
NP_000700.1:p.Thr338Asn
|
|
NM_001164783.2:c.1010C>A
|
NP_001158255.1:p.Thr337Asn
|
|