ENST00000251810.8:c.1042G>T
MANE Select
|
ENSP00000251810.3:p.Asp348Tyr
|
|
ENST00000251810.7:c.1042G>T
|
ENSP00000251810.3:p.Asp348Tyr
|
|
ENST00000395910.6:n.429G>T
|
|
|
ENST00000395912.6:c.886G>T
|
ENSP00000379248.2:p.Asp296Tyr
|
|
ENST00000519317.5:c.406G>T
|
ENSP00000430641.1:p.Asp136Tyr
|
|
ENST00000519962.5:c.187G>T
|
ENSP00000429140.1:p.Asp63Tyr
|
|
ENST00000522368.5:c.1211G>T
|
|
|
ENST00000522394.1:c.375G>T
|
ENSP00000429578.1:n.375G>T
|
|
ENST00000621845.1:c.880G>T
|
ENSP00000484318.1:p.Asp294Tyr
|
|
NM_001172477.1:c.1258G>T , LRG_788t1:c.1258G>T
|
NP_001165948.1:p.Asp420Tyr
|
|
NM_001172478.1:c.886G>T
|
NP_001165949.1:p.Asp296Tyr
|
|
NM_015713.4:c.1042G>T , LRG_788t2:c.1042G>T
|
NP_056528.2:p.Asp348Tyr
|
|
NM_001172478.2:c.886G>T
|
NP_001165949.1:p.Asp296Tyr
|
|
NM_015713.5:c.1042G>T
MANE Select
|
NP_056528.2:p.Asp348Tyr
|
|