ENST00000302850.10:c.3109G=
MANE Select
|
ENSP00000303830.4:p.Val1037=
|
|
ENST00000302850.9:c.3109G=
|
ENSP00000303830.4:p.Val1037=
|
|
ENST00000341500.9:c.3073G=
|
ENSP00000342838.4:p.Val1025=
|
|
NM_000208.2:c.3109G=
|
NP_000199.2:p.Val1037=
|
|
NM_000208.3:c.3109G=
|
NP_000199.2:p.Val1037=
|
|
NM_001079817.1:c.3073G=
|
NP_001073285.1:p.Val1025=
|
|
NM_001079817.2:c.3073G=
|
NP_001073285.1:p.Val1025=
|
|
XM_011527988.1:c.3184G=
|
XP_011526290.1:p.Val1062=
|
|
XM_011527989.1:c.3148G=
|
XP_011526291.1:p.Val1050=
|
|
XM_011527988.2:c.3106G=
|
XP_011526290.2:p.Val1036=
|
|
XM_011527989.3:c.3070G=
|
XP_011526291.2:p.Val1024=
|
|
NM_000208.4:c.3109G=
MANE Select
|
NP_000199.2:p.Val1037=
|
|
NM_001079817.3:c.3073G=
|
NP_001073285.1:p.Val1025=
|
|