ENST00000302850.10:c.2927A>G
MANE Select
|
ENSP00000303830.4:p.Tyr976Cys
|
|
ENST00000302850.9:c.2927A>G
|
ENSP00000303830.4:p.Tyr976Cys
|
|
ENST00000341500.9:c.2891A>G
|
ENSP00000342838.4:p.Tyr964Cys
|
|
NM_000208.2:c.2927A>G
|
NP_000199.2:p.Tyr976Cys
|
|
NM_000208.3:c.2927A>G
|
NP_000199.2:p.Tyr976Cys
|
|
NM_001079817.1:c.2891A>G
|
NP_001073285.1:p.Tyr964Cys
|
|
NM_001079817.2:c.2891A>G
|
NP_001073285.1:p.Tyr964Cys
|
|
XM_011527988.1:c.3002A>G
|
XP_011526290.1:p.Tyr1001Cys
|
|
XM_011527989.1:c.2966A>G
|
XP_011526291.1:p.Tyr989Cys
|
|
XM_011527988.2:c.2924A>G
|
XP_011526290.2:p.Tyr975Cys
|
|
XM_011527989.3:c.2888A>G
|
XP_011526291.2:p.Tyr963Cys
|
|
NM_000208.4:c.2927A>G
MANE Select
|
NP_000199.2:p.Tyr976Cys
|
|
NM_001079817.3:c.2891A>G
|
NP_001073285.1:p.Tyr964Cys
|
|