ENST00000585465.3:c.*2856T>G
|
ENSP00000490268.2:n.*2856T>G
|
|
ENST00000585748.3:c.883T>G
|
ENSP00000477641.2:p.Ser295Ala
|
|
ENST00000585851.2:c.1081T>G
|
ENSP00000467912.2:p.Ser361Ala
|
|
ENST00000326873.12:c.1255T>G
MANE Select
|
ENSP00000324856.6:p.Ser419Ala
|
|
ENST00000326873.11:c.1255T>G
|
ENSP00000324856.6:p.Ser419Ala
|
|
ENST00000585465.2:n.2988T>G
|
|
|
ENST00000586243.5:c.1254T>G
|
ENSP00000467240.2:p.Ala418=
|
|
ENST00000589152.5:n.1953T>G
|
|
|
NM_000455.4:c.1255T>G , LRG_319t1:c.1255T>G
|
NP_000446.1:p.Ser419Ala
|
|
XM_005259617.1:c.1250T>G
|
XP_005259674.1:p.Leu417Arg
|
|
XM_011528209.1:c.1028T>G
|
XP_011526511.1:p.Leu343Arg
|
|
XM_005259617.3:c.1250T>G
|
XP_005259674.1:p.Leu417Arg
|
|
XM_011528209.2:c.1028T>G
|
XP_011526511.1:p.Leu343Arg
|
|
XR_001753738.2:n.2061T>G
|
|
|
XR_001753740.2:n.2031T>G
|
|
|
NM_000455.5:c.1255T>G
MANE Select
|
NP_000446.1:p.Ser419Ala
|
|