ENST00000426263.10:c.760G=
MANE Select
|
ENSP00000416293.2:p.Glu254=
|
|
ENST00000669445.1:c.90G=
|
|
|
ENST00000674765.1:c.760G=
|
ENSP00000501811.1:p.Glu254=
|
|
ENST00000675112.1:n.783G=
|
|
|
ENST00000676254.1:n.1209G=
|
|
|
ENST00000426263.7:c.760G=
|
ENSP00000416293.2:p.Glu254=
|
|
ENST00000439722.2:c.639G=
|
ENSP00000395521.2:n.639G=
|
|
ENST00000475162.3:c.415+926G=
|
|
|
ENST00000630287.2:c.*75G=
|
ENSP00000486694.1:n.*75G=
|
|
NM_006516.2:c.760G=
|
NP_006507.2:p.Glu254=
|
|
NM_006516.3:c.760G=
|
NP_006507.2:p.Glu254=
|
|
NM_006516.4:c.760G=
MANE Select
|
NP_006507.2:p.Glu254=
|
|