ENST00000302850.10:c.3030G>C
MANE Select
|
ENSP00000303830.4:p.Val1010=
|
|
ENST00000302850.9:c.3030G>C
|
ENSP00000303830.4:p.Val1010=
|
|
ENST00000341500.9:c.2994G>C
|
ENSP00000342838.4:p.Val998=
|
|
NM_000208.2:c.3030G>C
|
NP_000199.2:p.Val1010=
|
|
NM_000208.3:c.3030G>C
|
NP_000199.2:p.Val1010=
|
|
NM_001079817.1:c.2994G>C
|
NP_001073285.1:p.Val998=
|
|
NM_001079817.2:c.2994G>C
|
NP_001073285.1:p.Val998=
|
|
XM_011527988.1:c.3105G>C
|
XP_011526290.1:p.Val1035=
|
|
XM_011527989.1:c.3069G>C
|
XP_011526291.1:p.Val1023=
|
|
XM_011527988.2:c.3027G>C
|
XP_011526290.2:p.Val1009=
|
|
XM_011527989.3:c.2991G>C
|
XP_011526291.2:p.Val997=
|
|
NM_000208.4:c.3030G>C
MANE Select
|
NP_000199.2:p.Val1010=
|
|
NM_001079817.3:c.2994G>C
|
NP_001073285.1:p.Val998=
|
|