ENST00000251810.8:c.147C>G
MANE Select
|
ENSP00000251810.3:p.Tyr49Ter
|
|
ENST00000251810.7:c.147C>G
|
ENSP00000251810.3:p.Tyr49Ter
|
|
ENST00000395912.6:c.49-6172C>G
|
ENSP00000379248.2:n.49-6172C>G
|
|
ENST00000517517.1:n.456C>G
|
|
|
ENST00000519317.5:c.48+6621C>G
|
ENSP00000430641.1:n.48+6621C>G
|
|
ENST00000519962.5:c.48+6621C>G
|
ENSP00000429140.1:n.48+6621C>G
|
|
ENST00000522368.5:c.316C>G
|
|
|
ENST00000522394.1:c.122+25C>G
|
ENSP00000429578.1:n.122+25C>G
|
|
ENST00000523957.1:c.*70C>G
|
ENSP00000427830.1:n.*70C>G
|
|
ENST00000621845.1:c.-16C>G
|
ENSP00000484318.1:n.-16C>G
|
|
NM_001172477.1:c.363C>G , LRG_788t1:c.363C>G
|
NP_001165948.1:p.Tyr121Ter
|
|
NM_001172478.1:c.49-6172C>G
|
NP_001165949.1:n.49-6172C>G
|
|
NM_015713.4:c.147C>G , LRG_788t2:c.147C>G
|
NP_056528.2:p.Tyr49Ter
|
|
NM_001172478.2:c.49-6172C>G
|
NP_001165949.1:n.49-6172C>G
|
|
NM_015713.5:c.147C>G
MANE Select
|
NP_056528.2:p.Tyr49Ter
|
|