ENST00000357578.8:c.1316C>A
MANE Select
|
ENSP00000350191.3:p.Thr439Asn
|
|
ENST00000479394.2:n.431C>A
|
|
|
ENST00000672352.1:c.935C>A
|
ENSP00000500876.1:p.Thr312Asn
|
|
ENST00000672652.1:c.1279C>A
|
|
|
ENST00000348925.2:c.1355C>A
|
ENSP00000314649.3:p.Thr452Asn
|
|
ENST00000357578.7:c.1316C>A
|
ENSP00000350191.3:p.Thr439Asn
|
|
ENST00000479394.1:n.431C>A
|
|
|
ENST00000491546.5:c.1232C>A
|
ENSP00000417687.1:p.Thr411Asn
|
|
NM_001080.3:c.1316C>A
MANE Select
|
NP_001071.1:p.Thr439Asn
|
|
NM_170740.1:c.1355C>A
|
NP_733936.1:p.Thr452Asn
|
|
NM_001368954.1:c.1172C>A
|
NP_001355883.1:p.Thr391Asn
|
|