ENST00000302850.10:c.3032A>C
MANE Select
|
ENSP00000303830.4:p.Tyr1011Ser
|
|
ENST00000302850.9:c.3032A>C
|
ENSP00000303830.4:p.Tyr1011Ser
|
|
ENST00000341500.9:c.2996A>C
|
ENSP00000342838.4:p.Tyr999Ser
|
|
NM_000208.2:c.3032A>C
|
NP_000199.2:p.Tyr1011Ser
|
|
NM_000208.3:c.3032A>C
|
NP_000199.2:p.Tyr1011Ser
|
|
NM_001079817.1:c.2996A>C
|
NP_001073285.1:p.Tyr999Ser
|
|
NM_001079817.2:c.2996A>C
|
NP_001073285.1:p.Tyr999Ser
|
|
XM_011527988.1:c.3107A>C
|
XP_011526290.1:p.Tyr1036Ser
|
|
XM_011527989.1:c.3071A>C
|
XP_011526291.1:p.Tyr1024Ser
|
|
XM_011527988.2:c.3029A>C
|
XP_011526290.2:p.Tyr1010Ser
|
|
XM_011527989.3:c.2993A>C
|
XP_011526291.2:p.Tyr998Ser
|
|
NM_000208.4:c.3032A>C
MANE Select
|
NP_000199.2:p.Tyr1011Ser
|
|
NM_001079817.3:c.2996A>C
|
NP_001073285.1:p.Tyr999Ser
|
|