ENST00000371820.4:c.1329A=
|
ENSP00000360885.4:p.Glu443=
|
|
ENST00000371817.8:c.1329A=
MANE Select
|
ENSP00000360882.3:p.Glu443=
|
|
ENST00000371817.7:c.1329A=
|
ENSP00000360882.3:p.Glu443=
|
|
ENST00000469093.1:n.68A=
|
|
|
ENST00000618395.4:c.1329A=
|
ENSP00000481360.1:p.Glu443=
|
|
NM_000093.4:c.1329A=
|
NP_000084.3:p.Glu443=
|
|
NM_001278074.1:c.1329A=
|
NP_001265003.1:p.Glu443=
|
|
XR_929712.1:n.1731A=
|
|
|
XR_929713.1:n.1731A=
|
|
|
XM_017014266.2:c.1329A=
|
XP_016869755.1:p.Glu443=
|
|
XR_001746183.1:n.1727A=
|
|
|
NM_000093.5:c.1329A=
MANE Select
|
NP_000084.3:p.Glu443=
|
|