ENST00000302850.10:c.4012G>T
MANE Select
|
ENSP00000303830.4:p.Glu1338Ter
|
|
ENST00000302850.9:c.4012G>T
|
ENSP00000303830.4:p.Glu1338Ter
|
|
ENST00000341500.9:c.3976G>T
|
ENSP00000342838.4:p.Glu1326Ter
|
|
NM_000208.2:c.4012G>T
|
NP_000199.2:p.Glu1338Ter
|
|
NM_000208.3:c.4012G>T
|
NP_000199.2:p.Glu1338Ter
|
|
NM_001079817.1:c.3976G>T
|
NP_001073285.1:p.Glu1326Ter
|
|
NM_001079817.2:c.3976G>T
|
NP_001073285.1:p.Glu1326Ter
|
|
XM_011527988.1:c.4087G>T
|
XP_011526290.1:p.Glu1363Ter
|
|
XM_011527989.1:c.4051G>T
|
XP_011526291.1:p.Glu1351Ter
|
|
XM_011527988.2:c.4009G>T
|
XP_011526290.2:p.Glu1337Ter
|
|
XM_011527989.3:c.3973G>T
|
XP_011526291.2:p.Glu1325Ter
|
|
NM_000208.4:c.4012G>T
MANE Select
|
NP_000199.2:p.Glu1338Ter
|
|
NM_001079817.3:c.3976G>T
|
NP_001073285.1:p.Glu1326Ter
|
|