ENST00000302850.10:c.3852G>T
MANE Select
|
ENSP00000303830.4:p.Leu1284=
|
|
ENST00000302850.9:c.3852G>T
|
ENSP00000303830.4:p.Leu1284=
|
|
ENST00000341500.9:c.3816G>T
|
ENSP00000342838.4:p.Leu1272=
|
|
NM_000208.2:c.3852G>T
|
NP_000199.2:p.Leu1284=
|
|
NM_000208.3:c.3852G>T
|
NP_000199.2:p.Leu1284=
|
|
NM_001079817.1:c.3816G>T
|
NP_001073285.1:p.Leu1272=
|
|
NM_001079817.2:c.3816G>T
|
NP_001073285.1:p.Leu1272=
|
|
XM_011527988.1:c.3927G>T
|
XP_011526290.1:p.Leu1309=
|
|
XM_011527989.1:c.3891G>T
|
XP_011526291.1:p.Leu1297=
|
|
XM_011527988.2:c.3849G>T
|
XP_011526290.2:p.Leu1283=
|
|
XM_011527989.3:c.3813G>T
|
XP_011526291.2:p.Leu1271=
|
|
NM_000208.4:c.3852G>T
MANE Select
|
NP_000199.2:p.Leu1284=
|
|
NM_001079817.3:c.3816G>T
|
NP_001073285.1:p.Leu1272=
|
|