ENST00000585465.3:c.*2842C>G
|
ENSP00000490268.2:n.*2842C>G
|
|
ENST00000585748.3:c.869C>G
|
ENSP00000477641.2:p.Ala290Gly
|
|
ENST00000585851.2:c.1067C>G
|
ENSP00000467912.2:p.Ala356Gly
|
|
ENST00000326873.12:c.1241C>G
MANE Select
|
ENSP00000324856.6:p.Ala414Gly
|
|
ENST00000326873.11:c.1241C>G
|
ENSP00000324856.6:p.Ala414Gly
|
|
ENST00000585465.2:n.2974C>G
|
|
|
ENST00000586243.5:c.1240C>G
|
ENSP00000467240.2:p.Pro414Ala
|
|
ENST00000589152.5:n.1939C>G
|
|
|
NM_000455.4:c.1241C>G , LRG_319t1:c.1241C>G
|
NP_000446.1:p.Ala414Gly
|
|
XM_005259617.1:c.1236C>G
|
XP_005259674.1:p.Cys412Trp
|
|
XM_011528209.1:c.1014C>G
|
XP_011526511.1:p.Cys338Trp
|
|
XM_005259617.3:c.1236C>G
|
XP_005259674.1:p.Cys412Trp
|
|
XM_011528209.2:c.1014C>G
|
XP_011526511.1:p.Cys338Trp
|
|
XR_001753738.2:n.2047C>G
|
|
|
XR_001753740.2:n.2017C>G
|
|
|
NM_000455.5:c.1241C>G
MANE Select
|
NP_000446.1:p.Ala414Gly
|
|