ENST00000251810.8:c.993T>G
MANE Select
|
ENSP00000251810.3:p.Tyr331Ter
|
|
ENST00000251810.7:c.993T>G
|
ENSP00000251810.3:p.Tyr331Ter
|
|
ENST00000395910.6:n.380T>G
|
|
|
ENST00000395912.6:c.837T>G
|
ENSP00000379248.2:p.Tyr279Ter
|
|
ENST00000519317.5:c.357T>G
|
ENSP00000430641.1:p.Tyr119Ter
|
|
ENST00000519962.5:c.138T>G
|
ENSP00000429140.1:p.Tyr46Ter
|
|
ENST00000522368.5:c.1162T>G
|
|
|
ENST00000522394.1:c.326T>G
|
ENSP00000429578.1:n.326T>G
|
|
ENST00000621845.1:c.831T>G
|
ENSP00000484318.1:p.Tyr277Ter
|
|
NM_001172477.1:c.1209T>G , LRG_788t1:c.1209T>G
|
NP_001165948.1:p.Tyr403Ter
|
|
NM_001172478.1:c.837T>G
|
NP_001165949.1:p.Tyr279Ter
|
|
NM_015713.4:c.993T>G , LRG_788t2:c.993T>G
|
NP_056528.2:p.Tyr331Ter
|
|
NM_001172478.2:c.837T>G
|
NP_001165949.1:p.Tyr279Ter
|
|
NM_015713.5:c.993T>G
MANE Select
|
NP_056528.2:p.Tyr331Ter
|
|