ENST00000426263.10:c.877T>G
MANE Select
|
ENSP00000416293.2:p.Tyr293Asp
|
|
ENST00000674545.1:n.195T>G
|
|
|
ENST00000674765.1:c.877T>G
|
ENSP00000501811.1:p.Tyr293Asp
|
|
ENST00000675112.1:n.1178T>G
|
|
|
ENST00000676254.1:n.1326T>G
|
|
|
ENST00000426263.7:c.877T>G
|
ENSP00000416293.2:p.Tyr293Asp
|
|
ENST00000439722.2:c.756T>G
|
ENSP00000395521.2:n.756T>G
|
|
ENST00000475162.3:c.415+1321T>G
|
|
|
ENST00000630287.2:c.*192T>G
|
ENSP00000486694.1:n.*192T>G
|
|
NM_006516.2:c.877T>G
|
NP_006507.2:p.Tyr293Asp
|
|
NM_006516.3:c.877T>G
|
NP_006507.2:p.Tyr293Asp
|
|
NM_006516.4:c.877T>G
MANE Select
|
NP_006507.2:p.Tyr293Asp
|
|