ENST00000302850.10:c.3069C>A
MANE Select
|
ENSP00000303830.4:p.Ile1023=
|
|
ENST00000302850.9:c.3069C>A
|
ENSP00000303830.4:p.Ile1023=
|
|
ENST00000341500.9:c.3033C>A
|
ENSP00000342838.4:p.Ile1011=
|
|
NM_000208.2:c.3069C>A
|
NP_000199.2:p.Ile1023=
|
|
NM_000208.3:c.3069C>A
|
NP_000199.2:p.Ile1023=
|
|
NM_001079817.1:c.3033C>A
|
NP_001073285.1:p.Ile1011=
|
|
NM_001079817.2:c.3033C>A
|
NP_001073285.1:p.Ile1011=
|
|
XM_011527988.1:c.3144C>A
|
XP_011526290.1:p.Ile1048=
|
|
XM_011527989.1:c.3108C>A
|
XP_011526291.1:p.Ile1036=
|
|
XM_011527988.2:c.3066C>A
|
XP_011526290.2:p.Ile1022=
|
|
XM_011527989.3:c.3030C>A
|
XP_011526291.2:p.Ile1010=
|
|
NM_000208.4:c.3069C>A
MANE Select
|
NP_000199.2:p.Ile1023=
|
|
NM_001079817.3:c.3033C>A
|
NP_001073285.1:p.Ile1011=
|
|