ENST00000691183.1:c.*401G=
|
ENSP00000509954.1:n.*401G=
|
|
ENST00000378842.8:c.813G=
MANE Select
|
ENSP00000368119.4:p.Glu271=
|
|
ENST00000378842.7:c.813G=
|
ENSP00000368119.3:p.Glu271=
|
|
ENST00000450095.6:c.486G=
|
ENSP00000401956.2:p.Glu162=
|
|
ENST00000473506.6:c.*401G=
|
ENSP00000432839.2:n.*401G=
|
|
ENST00000489643.6:n.893G=
|
|
|
ENST00000554085.5:c.*557G=
|
ENSP00000450419.1:n.*557G=
|
|
ENST00000554550.5:c.*433G=
|
ENSP00000451435.1:n.*433G=
|
|
ENST00000554638.5:n.1285G=
|
|
|
ENST00000555020.5:n.1274G=
|
|
|
ENST00000555086.5:n.817G=
|
|
|
ENST00000555754.1:n.158G=
|
|
|
ENST00000556244.1:c.800G=
|
|
|
ENST00000556278.1:c.432+431G=
|
ENSP00000451792.1:n.432+431G=
|
|
ENST00000557706.5:n.1375G=
|
|
|
NM_000155.3:c.813G=
|
NP_000146.2:p.Glu271=
|
|
NM_001258332.1:c.486G=
|
NP_001245261.1:p.Glu162=
|
|
NM_000155.4:c.813G=
MANE Select
|
NP_000146.2:p.Glu271=
|
|
NM_001258332.2:c.486G=
|
NP_001245261.1:p.Glu162=
|
|