ENST00000426263.10:c.874T>G
MANE Select
|
ENSP00000416293.2:p.Tyr292Asp
|
|
ENST00000674545.1:n.192T>G
|
|
|
ENST00000674765.1:c.874T>G
|
ENSP00000501811.1:p.Tyr292Asp
|
|
ENST00000675112.1:n.1175T>G
|
|
|
ENST00000676254.1:n.1323T>G
|
|
|
ENST00000426263.7:c.874T>G
|
ENSP00000416293.2:p.Tyr292Asp
|
|
ENST00000439722.2:c.753T>G
|
ENSP00000395521.2:n.753T>G
|
|
ENST00000475162.3:c.415+1318T>G
|
|
|
ENST00000630287.2:c.*189T>G
|
ENSP00000486694.1:n.*189T>G
|
|
NM_006516.2:c.874T>G
|
NP_006507.2:p.Tyr292Asp
|
|
NM_006516.3:c.874T>G
|
NP_006507.2:p.Tyr292Asp
|
|
NM_006516.4:c.874T>G
MANE Select
|
NP_006507.2:p.Tyr292Asp
|
|