ENST00000302068.9:c.1231G>A
MANE Select
|
ENSP00000306099.4:p.Asp411Asn
|
|
ENST00000302068.8:c.1231G>A
|
ENSP00000306099.4:p.Asp411Asn
|
|
ENST00000502545.5:n.939+479G>A
|
|
|
ENST00000509493.1:c.574G>A
|
ENSP00000426757.1:p.Asp192Asn
|
|
NM_001184741.1:c.1054G>A
|
NP_001171670.1:p.Asp352Asn
|
|
NM_005141.4:c.1231G>A , LRG_558t1:c.1231G>A
|
NP_005132.2:p.Asp411Asn
|
|
NM_001382759.1:c.1099G>A
|
NP_001369688.1:p.Asp367Asn
|
|
NM_001382760.1:c.1231G>A
|
NP_001369689.1:p.Asp411Asn
|
|
NM_001382761.1:c.1231G>A
|
NP_001369690.1:p.Asp411Asn
|
|
NM_001382762.1:c.931G>A
|
NP_001369691.1:p.Asp311Asn
|
|
NM_001382763.1:c.1222G>A
|
NP_001369692.1:p.Asp408Asn
|
|
NM_001382764.1:c.*5G>A
|
NP_001369693.1:n.*5G>A
|
|
NM_001382765.1:c.1220+11G>A
|
NP_001369694.1:n.1220+11G>A
|
|
NM_005141.5:c.1231G>A
MANE Select
|
NP_005132.2:p.Asp411Asn
|
|