ENST00000578493.2:n.1116G=
|
|
|
ENST00000699291.1:c.908G=
|
ENSP00000514272.1:n.908G=
|
|
ENST00000699292.1:n.1318G=
|
|
|
ENST00000225275.4:c.1783G=
MANE Select
|
ENSP00000225275.3:p.Gly595=
|
|
ENST00000225275.3:c.1783G=
|
ENSP00000225275.3:p.Gly595=
|
|
ENST00000577220.1:c.183+58G=
|
ENSP00000464668.1:n.183+58G=
|
|
NM_000250.1:c.1783G= , LRG_84t1:c.1783G=
|
NP_000241.1:p.Gly595=
|
|
XM_011524821.1:c.1969G=
|
XP_011523123.1:p.Gly657=
|
|
XM_011524822.1:c.1498G=
|
XP_011523124.1:p.Gly500=
|
|
NM_000250.2:c.1783G=
MANE Select
|
NP_000241.1:p.Gly595=
|
|