ENST00000302850.10:c.3860T>G
MANE Select
|
ENSP00000303830.4:p.Val1287Gly
|
|
ENST00000302850.9:c.3860T>G
|
ENSP00000303830.4:p.Val1287Gly
|
|
ENST00000341500.9:c.3824T>G
|
ENSP00000342838.4:p.Val1275Gly
|
|
NM_000208.2:c.3860T>G
|
NP_000199.2:p.Val1287Gly
|
|
NM_000208.3:c.3860T>G
|
NP_000199.2:p.Val1287Gly
|
|
NM_001079817.1:c.3824T>G
|
NP_001073285.1:p.Val1275Gly
|
|
NM_001079817.2:c.3824T>G
|
NP_001073285.1:p.Val1275Gly
|
|
XM_011527988.1:c.3935T>G
|
XP_011526290.1:p.Val1312Gly
|
|
XM_011527989.1:c.3899T>G
|
XP_011526291.1:p.Val1300Gly
|
|
XM_011527988.2:c.3857T>G
|
XP_011526290.2:p.Val1286Gly
|
|
XM_011527989.3:c.3821T>G
|
XP_011526291.2:p.Val1274Gly
|
|
NM_000208.4:c.3860T>G
MANE Select
|
NP_000199.2:p.Val1287Gly
|
|
NM_001079817.3:c.3824T>G
|
NP_001073285.1:p.Val1275Gly
|
|