ENST00000378823.8:c.3166G>T
MANE Select
|
ENSP00000368100.4:p.Glu1056Ter
|
|
ENST00000638452.2:c.2869G>T
|
ENSP00000492349.2:p.Glu957Ter
|
|
ENST00000638504.1:n.2774G>T
|
|
|
ENST00000638568.2:c.2869G>T
|
ENSP00000491158.2:p.Glu957Ter
|
|
ENST00000639899.1:n.3685G>T
|
|
|
ENST00000640655.2:c.2869G>T
|
ENSP00000491596.2:p.Glu957Ter
|
|
ENST00000651249.1:c.2G>T
|
|
|
ENST00000378823.7:c.3166G>T
|
ENSP00000368100.4:p.Glu1056Ter
|
|
ENST00000533482.5:c.*2792G>T
|
ENSP00000431225.1:n.*2792G>T
|
|
NM_005732.3:c.3166G>T
|
NP_005723.2:p.Glu1056Ter
|
|
NM_005732.4:c.3166G>T
MANE Select
|
NP_005723.2:p.Glu1056Ter
|
|