ENST00000330062.8:c.673G>A
MANE Select
|
ENSP00000331897.4:p.Asp225Asn
|
|
ENST00000330062.7:c.673G>A
|
ENSP00000331897.3:p.Asp225Asn
|
|
ENST00000540499.2:c.517G>A
|
ENSP00000446147.2:p.Asp173Asn
|
|
ENST00000559482.5:c.346G>A
|
ENSP00000453016.1:p.Asp116Asn
|
|
ENST00000560061.1:c.*298G>A
|
ENSP00000453254.1:n.*298G>A
|
|
NM_001289910.1:c.517G>A , LRG_611t1:c.517G>A
|
NP_001276839.1:p.Asp173Asn
|
|
NM_001290114.1:c.283G>A
|
NP_001277043.1:p.Asp95Asn
|
|
NM_002168.3:c.673G>A , LRG_611t2:c.673G>A
|
NP_002159.2:p.Asp225Asn
|
|
NM_001290114.2:c.283G>A
|
NP_001277043.1:p.Asp95Asn
|
|
NM_002168.4:c.673G>A
MANE Select
|
NP_002159.2:p.Asp225Asn
|
|