|
NM_006767.4:c.423T>G
MANE Select
|
NP_006758.2:p.Tyr141Ter
|
|
ENST00000646124.2:c.423T>G
MANE Select
|
ENSP00000496779.1:p.Tyr141Ter
|
|
NM_006767.3:c.423T>G
|
NP_006758.2:p.Tyr141Ter
|
|
ENST00000215739.12:c.423T>G
|
ENSP00000215739.8:p.Tyr141Ter
|
|
ENST00000414985.5:c.343T>G
|
ENSP00000397247.1:p.Phe115Val
|
|
ENST00000443265.5:c.*122T>G
|
ENSP00000406466.1:n.*122T>G
|
|
ENST00000479606.5:n.569T>G
|
|
|
ENST00000480895.1:n.119T>G
|
|
|
ENST00000642151.1:c.254T>G
|
|
|
ENST00000644435.1:c.329T>G
|
|
|
ENST00000645935.1:c.366T>G
|
ENSP00000493479.1:p.Tyr122Ter
|
|
ENST00000646506.1:n.2T>G
|
|
|
ENST00000700578.1:c.423T>G
|
ENSP00000515073.1:p.Tyr141Ter
|