ENST00000302068.9:c.1153G>T
MANE Select
|
ENSP00000306099.4:p.Asp385Tyr
|
|
ENST00000302068.8:c.1153G>T
|
ENSP00000306099.4:p.Asp385Tyr
|
|
ENST00000502545.5:n.939+401G>T
|
|
|
ENST00000509493.1:c.496G>T
|
ENSP00000426757.1:p.Asp166Tyr
|
|
NM_001184741.1:c.976G>T
|
NP_001171670.1:p.Asp326Tyr
|
|
NM_005141.4:c.1153G>T , LRG_558t1:c.1153G>T
|
NP_005132.2:p.Asp385Tyr
|
|
NM_001382759.1:c.1021G>T
|
NP_001369688.1:p.Asp341Tyr
|
|
NM_001382760.1:c.1153G>T
|
NP_001369689.1:p.Asp385Tyr
|
|
NM_001382761.1:c.1153G>T
|
NP_001369690.1:p.Asp385Tyr
|
|
NM_001382762.1:c.853G>T
|
NP_001369691.1:p.Asp285Tyr
|
|
NM_001382763.1:c.1144G>T
|
NP_001369692.1:p.Asp382Tyr
|
|
NM_001382764.1:c.1081-65G>T
|
NP_001369693.1:n.1081-65G>T
|
|
NM_001382765.1:c.1153G>T
|
NP_001369694.1:p.Asp385Tyr
|
|
NM_005141.5:c.1153G>T
MANE Select
|
NP_005132.2:p.Asp385Tyr
|
|