ENST00000302850.10:c.3162G>C
MANE Select
|
ENSP00000303830.4:p.Val1054=
|
|
ENST00000302850.9:c.3162G>C
|
ENSP00000303830.4:p.Val1054=
|
|
ENST00000341500.9:c.3126G>C
|
ENSP00000342838.4:p.Val1042=
|
|
ENST00000593970.1:n.8G>C
|
|
|
NM_000208.2:c.3162G>C
|
NP_000199.2:p.Val1054=
|
|
NM_000208.3:c.3162G>C
|
NP_000199.2:p.Val1054=
|
|
NM_001079817.1:c.3126G>C
|
NP_001073285.1:p.Val1042=
|
|
NM_001079817.2:c.3126G>C
|
NP_001073285.1:p.Val1042=
|
|
XM_011527988.1:c.3237G>C
|
XP_011526290.1:p.Val1079=
|
|
XM_011527989.1:c.3201G>C
|
XP_011526291.1:p.Val1067=
|
|
XM_011527988.2:c.3159G>C
|
XP_011526290.2:p.Val1053=
|
|
XM_011527989.3:c.3123G>C
|
XP_011526291.2:p.Val1041=
|
|
NM_000208.4:c.3162G>C
MANE Select
|
NP_000199.2:p.Val1054=
|
|
NM_001079817.3:c.3126G>C
|
NP_001073285.1:p.Val1042=
|
|