ENST00000392676.8:c.4347G>C
MANE Select
|
ENSP00000376443.2:p.Gly1449=
|
|
ENST00000392676.7:c.4347G>C
|
ENSP00000376443.2:p.Gly1449=
|
|
ENST00000586811.1:c.1245G>C
|
ENSP00000465351.1:p.Gly415=
|
|
ENST00000586995.5:c.3409G>C
|
ENSP00000467251.1:n.3409G>C
|
|
ENST00000588877.5:c.4347G>C
|
ENSP00000467882.1:p.Gly1449=
|
|
ENST00000591234.5:c.2289G>C
|
ENSP00000465766.1:n.2289G>C
|
|
NM_018672.4:c.4347G>C
|
NP_061142.2:p.Gly1449=
|
|
NM_172232.3:c.4347G>C
|
NP_758424.1:p.Gly1449=
|
|
NM_172232.4:c.4347G>C
MANE Select
|
NP_758424.1:p.Gly1449=
|
|
NM_018672.5:c.4347G>C
|
NP_061142.2:p.Gly1449=
|
|