ENST00000262629.9:c.148G>T
MANE Select
|
ENSP00000262629.3:p.Asp50Tyr
|
|
ENST00000262629.8:c.148G>T
|
ENSP00000262629.3:p.Asp50Tyr
|
|
ENST00000424586.7:c.115G>T
|
ENSP00000402371.3:p.Asp39Tyr
|
|
ENST00000544690.6:c.115G>T
|
ENSP00000445332.1:p.Asp39Tyr
|
|
ENST00000585626.1:n.215G>T
|
|
|
ENST00000585901.6:c.148G>T
|
ENSP00000468608.1:p.Asp50Tyr
|
|
ENST00000586946.1:c.*33G>T
|
ENSP00000465656.1:n.*33G>T
|
|
ENST00000587837.5:c.*33G>T
|
ENSP00000465081.1:n.*33G>T
|
|
ENST00000588439.1:n.292G>T
|
|
|
ENST00000589517.1:c.148G>T
|
ENSP00000468447.1:p.Asp50Tyr
|
|
NM_001173514.1:c.115G>T
|
NP_001166985.1:p.Asp39Tyr
|
|
NM_001173515.1:c.115G>T
|
NP_001166986.1:p.Asp39Tyr
|
|
NM_003332.3:c.148G>T , LRG_607t1:c.148G>T
|
NP_003323.1:p.Asp50Tyr
|
|
NM_198125.2:c.148G>T
|
NP_937758.1:p.Asp50Tyr
|
|
NR_033390.1:n.189G>T
|
|
|
NM_001173514.2:c.115G>T
|
NP_001166985.1:p.Asp39Tyr
|
|
NM_001173515.2:c.115G>T
|
NP_001166986.1:p.Asp39Tyr
|
|
NM_003332.4:c.148G>T
MANE Select
|
NP_003323.1:p.Asp50Tyr
|
|
NM_198125.3:c.148G>T
|
NP_937758.1:p.Asp50Tyr
|
|
NR_033390.2:n.175G>T
|
|
|