ENST00000225964.10:c.3825G>A
MANE Select
|
ENSP00000225964.6:p.Trp1275Ter
|
|
ENST00000225964.9:c.3825G>A
|
ENSP00000225964.5:p.Trp1275Ter
|
|
ENST00000510710.3:n.494G>A
|
|
|
NM_000088.3:c.3825G>A , LRG_1t1:c.3825G>A
|
NP_000079.2:p.Trp1275Ter
|
|
XM_005257058.3:c.3555G>A
|
XP_005257115.2:p.Trp1185Ter
|
|
XM_005257059.3:c.2907G>A
|
XP_005257116.2:p.Trp969Ter
|
|
XM_011524341.1:c.3627G>A
|
XP_011522643.1:p.Trp1209Ter
|
|
XM_005257058.4:c.3555G>A
|
XP_005257115.2:p.Trp1185Ter
|
|
XM_005257059.4:c.2907G>A
|
XP_005257116.2:p.Trp969Ter
|
|
NM_000088.4:c.3825G>A
MANE Select
|
NP_000079.2:p.Trp1275Ter
|
|