ENST00000302850.10:c.4115G>A
MANE Select
|
ENSP00000303830.4:p.Arg1372Gln
|
|
ENST00000302850.9:c.4115G>A
|
ENSP00000303830.4:p.Arg1372Gln
|
|
ENST00000341500.9:c.4079G>A
|
ENSP00000342838.4:p.Arg1360Gln
|
|
NM_000208.2:c.4115G>A
|
NP_000199.2:p.Arg1372Gln
|
|
NM_000208.3:c.4115G>A
|
NP_000199.2:p.Arg1372Gln
|
|
NM_001079817.1:c.4079G>A
|
NP_001073285.1:p.Arg1360Gln
|
|
NM_001079817.2:c.4079G>A
|
NP_001073285.1:p.Arg1360Gln
|
|
XM_011527988.1:c.4190G>A
|
XP_011526290.1:p.Arg1397Gln
|
|
XM_011527989.1:c.4154G>A
|
XP_011526291.1:p.Arg1385Gln
|
|
XM_011527988.2:c.4112G>A
|
XP_011526290.2:p.Arg1371Gln
|
|
XM_011527989.3:c.4076G>A
|
XP_011526291.2:p.Arg1359Gln
|
|
NM_000208.4:c.4115G>A
MANE Select
|
NP_000199.2:p.Arg1372Gln
|
|
NM_001079817.3:c.4079G>A
|
NP_001073285.1:p.Arg1360Gln
|
|