ENST00000225964.10:c.1475G=
MANE Select
|
ENSP00000225964.6:p.Ser492=
|
|
ENST00000225964.9:c.1475G=
|
ENSP00000225964.5:p.Ser492=
|
|
ENST00000471344.1:n.419G=
|
|
|
NM_000088.3:c.1475G= , LRG_1t1:c.1475G=
|
NP_000079.2:p.Ser492=
|
|
XM_005257058.3:c.1475G=
|
XP_005257115.2:p.Ser492=
|
|
XM_005257059.3:c.957+1701G=
|
XP_005257116.2:n.957+1701G=
|
|
XM_011524341.1:c.1277G=
|
XP_011522643.1:p.Ser426=
|
|
XM_005257058.4:c.1475G=
|
XP_005257115.2:p.Ser492=
|
|
XM_005257059.4:c.957+1701G=
|
XP_005257116.2:n.957+1701G=
|
|
NM_000088.4:c.1475G=
MANE Select
|
NP_000079.2:p.Ser492=
|
|