ENST00000396623.8:c.1046A>C
MANE Select
|
ENSP00000379865.3:p.Asn349Thr
|
|
ENST00000648156.1:c.*265A>C
|
ENSP00000497007.1:n.*265A>C
|
|
ENST00000276576.11:c.*882A>C
|
ENSP00000276576.7:n.*882A>C
|
|
ENST00000396623.7:c.1046A>C
|
ENSP00000379865.3:p.Asn349Thr
|
|
ENST00000415254.5:c.902A>C
|
ENSP00000407115.1:p.Asn301Thr
|
|
ENST00000419955.5:c.*1055A>C
|
ENSP00000392040.1:n.*1055A>C
|
|
ENST00000424777.6:c.*483A>C
|
ENSP00000410883.2:n.*483A>C
|
|
ENST00000426810.5:c.*1231A>C
|
ENSP00000406905.1:n.*1231A>C
|
|
ENST00000480040.5:n.121A>C
|
|
|
ENST00000496501.5:n.920A>C
|
|
|
NM_144650.2:c.1046A>C
|
NP_653251.2:p.Asn349Thr
|
|
NM_144650.3:c.1046A>C
MANE Select
|
NP_653251.2:p.Asn349Thr
|
|