ENST00000302850.10:c.3860T>A
MANE Select
|
ENSP00000303830.4:p.Val1287Asp
|
|
ENST00000302850.9:c.3860T>A
|
ENSP00000303830.4:p.Val1287Asp
|
|
ENST00000341500.9:c.3824T>A
|
ENSP00000342838.4:p.Val1275Asp
|
|
NM_000208.2:c.3860T>A
|
NP_000199.2:p.Val1287Asp
|
|
NM_000208.3:c.3860T>A
|
NP_000199.2:p.Val1287Asp
|
|
NM_001079817.1:c.3824T>A
|
NP_001073285.1:p.Val1275Asp
|
|
NM_001079817.2:c.3824T>A
|
NP_001073285.1:p.Val1275Asp
|
|
XM_011527988.1:c.3935T>A
|
XP_011526290.1:p.Val1312Asp
|
|
XM_011527989.1:c.3899T>A
|
XP_011526291.1:p.Val1300Asp
|
|
XM_011527988.2:c.3857T>A
|
XP_011526290.2:p.Val1286Asp
|
|
XM_011527989.3:c.3821T>A
|
XP_011526291.2:p.Val1274Asp
|
|
NM_000208.4:c.3860T>A
MANE Select
|
NP_000199.2:p.Val1287Asp
|
|
NM_001079817.3:c.3824T>A
|
NP_001073285.1:p.Val1275Asp
|
|