ENST00000302850.10:c.3072C>G
MANE Select
|
ENSP00000303830.4:p.Thr1024=
|
|
ENST00000302850.9:c.3072C>G
|
ENSP00000303830.4:p.Thr1024=
|
|
ENST00000341500.9:c.3036C>G
|
ENSP00000342838.4:p.Thr1012=
|
|
NM_000208.2:c.3072C>G
|
NP_000199.2:p.Thr1024=
|
|
NM_000208.3:c.3072C>G
|
NP_000199.2:p.Thr1024=
|
|
NM_001079817.1:c.3036C>G
|
NP_001073285.1:p.Thr1012=
|
|
NM_001079817.2:c.3036C>G
|
NP_001073285.1:p.Thr1012=
|
|
XM_011527988.1:c.3147C>G
|
XP_011526290.1:p.Thr1049=
|
|
XM_011527989.1:c.3111C>G
|
XP_011526291.1:p.Thr1037=
|
|
XM_011527988.2:c.3069C>G
|
XP_011526290.2:p.Thr1023=
|
|
XM_011527989.3:c.3033C>G
|
XP_011526291.2:p.Thr1011=
|
|
NM_000208.4:c.3072C>G
MANE Select
|
NP_000199.2:p.Thr1024=
|
|
NM_001079817.3:c.3036C>G
|
NP_001073285.1:p.Thr1012=
|
|