ENST00000302850.10:c.4133G>A
MANE Select
|
ENSP00000303830.4:p.Arg1378Gln
|
|
ENST00000302850.9:c.4133G>A
|
ENSP00000303830.4:p.Arg1378Gln
|
|
ENST00000341500.9:c.4097G>A
|
ENSP00000342838.4:p.Arg1366Gln
|
|
NM_000208.2:c.4133G>A
|
NP_000199.2:p.Arg1378Gln
|
|
NM_000208.3:c.4133G>A
|
NP_000199.2:p.Arg1378Gln
|
|
NM_001079817.1:c.4097G>A
|
NP_001073285.1:p.Arg1366Gln
|
|
NM_001079817.2:c.4097G>A
|
NP_001073285.1:p.Arg1366Gln
|
|
XM_011527988.1:c.4208G>A
|
XP_011526290.1:p.Arg1403Gln
|
|
XM_011527989.1:c.4172G>A
|
XP_011526291.1:p.Arg1391Gln
|
|
XM_011527988.2:c.4130G>A
|
XP_011526290.2:p.Arg1377Gln
|
|
XM_011527989.3:c.4094G>A
|
XP_011526291.2:p.Arg1365Gln
|
|
NM_000208.4:c.4133G>A
MANE Select
|
NP_000199.2:p.Arg1378Gln
|
|
NM_001079817.3:c.4097G>A
|
NP_001073285.1:p.Arg1366Gln
|
|