ENST00000302850.10:c.3853G>A
MANE Select
|
ENSP00000303830.4:p.Glu1285Lys
|
|
ENST00000302850.9:c.3853G>A
|
ENSP00000303830.4:p.Glu1285Lys
|
|
ENST00000341500.9:c.3817G>A
|
ENSP00000342838.4:p.Glu1273Lys
|
|
NM_000208.2:c.3853G>A
|
NP_000199.2:p.Glu1285Lys
|
|
NM_000208.3:c.3853G>A
|
NP_000199.2:p.Glu1285Lys
|
|
NM_001079817.1:c.3817G>A
|
NP_001073285.1:p.Glu1273Lys
|
|
NM_001079817.2:c.3817G>A
|
NP_001073285.1:p.Glu1273Lys
|
|
XM_011527988.1:c.3928G>A
|
XP_011526290.1:p.Glu1310Lys
|
|
XM_011527989.1:c.3892G>A
|
XP_011526291.1:p.Glu1298Lys
|
|
XM_011527988.2:c.3850G>A
|
XP_011526290.2:p.Glu1284Lys
|
|
XM_011527989.3:c.3814G>A
|
XP_011526291.2:p.Glu1272Lys
|
|
NM_000208.4:c.3853G>A
MANE Select
|
NP_000199.2:p.Glu1285Lys
|
|
NM_001079817.3:c.3817G>A
|
NP_001073285.1:p.Glu1273Lys
|
|