ENST00000330062.8:c.669C=
MANE Select
|
ENSP00000331897.4:p.Asn223=
|
|
ENST00000330062.7:c.669C=
|
ENSP00000331897.3:p.Asn223=
|
|
ENST00000540499.2:c.513C=
|
ENSP00000446147.2:p.Asn171=
|
|
ENST00000559482.5:c.342C=
|
ENSP00000453016.1:p.Asn114=
|
|
ENST00000560061.1:c.*294C=
|
ENSP00000453254.1:n.*294C=
|
|
NM_001289910.1:c.513C= , LRG_611t1:c.513C=
|
NP_001276839.1:p.Asn171=
|
|
NM_001290114.1:c.279C=
|
NP_001277043.1:p.Asn93=
|
|
NM_002168.3:c.669C= , LRG_611t2:c.669C=
|
NP_002159.2:p.Asn223=
|
|
NM_001290114.2:c.279C=
|
NP_001277043.1:p.Asn93=
|
|
NM_002168.4:c.669C=
MANE Select
|
NP_002159.2:p.Asn223=
|
|