ENST00000251810.8:c.1024G>T
MANE Select
|
ENSP00000251810.3:p.Asp342Tyr
|
|
ENST00000251810.7:c.1024G>T
|
ENSP00000251810.3:p.Asp342Tyr
|
|
ENST00000395910.6:n.411G>T
|
|
|
ENST00000395912.6:c.868G>T
|
ENSP00000379248.2:p.Asp290Tyr
|
|
ENST00000519317.5:c.388G>T
|
ENSP00000430641.1:p.Asp130Tyr
|
|
ENST00000519962.5:c.169G>T
|
ENSP00000429140.1:p.Asp57Tyr
|
|
ENST00000522368.5:c.1193G>T
|
|
|
ENST00000522394.1:c.357G>T
|
ENSP00000429578.1:n.357G>T
|
|
ENST00000621845.1:c.862G>T
|
ENSP00000484318.1:p.Asp288Tyr
|
|
NM_001172477.1:c.1240G>T , LRG_788t1:c.1240G>T
|
NP_001165948.1:p.Asp414Tyr
|
|
NM_001172478.1:c.868G>T
|
NP_001165949.1:p.Asp290Tyr
|
|
NM_015713.4:c.1024G>T , LRG_788t2:c.1024G>T
|
NP_056528.2:p.Asp342Tyr
|
|
NM_001172478.2:c.868G>T
|
NP_001165949.1:p.Asp290Tyr
|
|
NM_015713.5:c.1024G>T
MANE Select
|
NP_056528.2:p.Asp342Tyr
|
|