ENST00000480266.6:c.-281G=
|
ENSP00000479015.1:n.-281G=
|
|
ENST00000373203.9:c.266G=
MANE Select
|
ENSP00000362299.4:p.Gly89=
|
|
ENST00000344849.4:c.266G=
|
ENSP00000341917.3:p.Gly89=
|
|
ENST00000373203.8:c.266G=
|
ENSP00000362299.4:p.Gly89=
|
|
ENST00000462196.1:n.24G=
|
|
|
ENST00000480266.5:c.-281G=
|
ENSP00000479015.1:n.-281G=
|
|
NM_000118.3:c.266G= , LRG_589t1:c.266G=
|
NP_000109.1:p.Gly89=
|
|
NM_001114753.2:c.266G= , LRG_589t2:c.266G=
|
NP_001108225.1:p.Gly89=
|
|
NM_001278138.1:c.-281G=
|
NP_001265067.1:n.-281G=
|
|
XR_001746952.2:n.83-2617C=
|
|
|
NM_001114753.3:c.266G=
MANE Select
|
NP_001108225.1:p.Gly89=
|
|
NM_001278138.2:c.-281G=
|
NP_001265067.1:n.-281G=
|
|