|
NM_006767.4:c.357C>A
MANE Select
|
NP_006758.2:p.Tyr119Ter
|
|
ENST00000646124.2:c.357C>A
MANE Select
|
ENSP00000496779.1:p.Tyr119Ter
|
|
NM_006767.3:c.357C>A
|
NP_006758.2:p.Tyr119Ter
|
|
ENST00000215739.12:c.357C>A
|
ENSP00000215739.8:p.Tyr119Ter
|
|
ENST00000414985.5:c.321-470C>A
|
ENSP00000397247.1:n.321-470C>A
|
|
ENST00000443265.5:c.*56C>A
|
ENSP00000406466.1:n.*56C>A
|
|
ENST00000479606.5:n.503C>A
|
|
|
ENST00000480895.1:n.97-470C>A
|
|
|
ENST00000642151.1:c.232-470C>A
|
|
|
ENST00000644435.1:c.263C>A
|
|
|
ENST00000645935.1:c.300C>A
|
ENSP00000493479.1:p.Tyr100Ter
|
|
ENST00000700578.1:c.357C>A
|
ENSP00000515073.1:p.Tyr119Ter
|