ENST00000302850.10:c.3919G>C
MANE Select
|
ENSP00000303830.4:p.Glu1307Gln
|
|
ENST00000302850.9:c.3919G>C
|
ENSP00000303830.4:p.Glu1307Gln
|
|
ENST00000341500.9:c.3883G>C
|
ENSP00000342838.4:p.Glu1295Gln
|
|
NM_000208.2:c.3919G>C
|
NP_000199.2:p.Glu1307Gln
|
|
NM_000208.3:c.3919G>C
|
NP_000199.2:p.Glu1307Gln
|
|
NM_001079817.1:c.3883G>C
|
NP_001073285.1:p.Glu1295Gln
|
|
NM_001079817.2:c.3883G>C
|
NP_001073285.1:p.Glu1295Gln
|
|
XM_011527988.1:c.3994G>C
|
XP_011526290.1:p.Glu1332Gln
|
|
XM_011527989.1:c.3958G>C
|
XP_011526291.1:p.Glu1320Gln
|
|
XM_011527988.2:c.3916G>C
|
XP_011526290.2:p.Glu1306Gln
|
|
XM_011527989.3:c.3880G>C
|
XP_011526291.2:p.Glu1294Gln
|
|
NM_000208.4:c.3919G>C
MANE Select
|
NP_000199.2:p.Glu1307Gln
|
|
NM_001079817.3:c.3883G>C
|
NP_001073285.1:p.Glu1295Gln
|
|