ENST00000585465.3:c.*2840T>A
|
ENSP00000490268.2:n.*2840T>A
|
|
ENST00000585748.3:c.867T>A
|
ENSP00000477641.2:p.Pro289=
|
|
ENST00000585851.2:c.1065T>A
|
ENSP00000467912.2:p.Pro355=
|
|
ENST00000326873.12:c.1239T>A
MANE Select
|
ENSP00000324856.6:p.Pro413=
|
|
ENST00000326873.11:c.1239T>A
|
ENSP00000324856.6:p.Pro413=
|
|
ENST00000585465.2:n.2972T>A
|
|
|
ENST00000586243.5:c.1238T>A
|
ENSP00000467240.2:p.Leu413Gln
|
|
ENST00000589152.5:n.1937T>A
|
|
|
NM_000455.4:c.1239T>A , LRG_319t1:c.1239T>A
|
NP_000446.1:p.Pro413=
|
|
XM_005259617.1:c.1234T>A
|
XP_005259674.1:p.Cys412Ser
|
|
XM_011528209.1:c.1012T>A
|
XP_011526511.1:p.Cys338Ser
|
|
XM_005259617.3:c.1234T>A
|
XP_005259674.1:p.Cys412Ser
|
|
XM_011528209.2:c.1012T>A
|
XP_011526511.1:p.Cys338Ser
|
|
XR_001753738.2:n.2045T>A
|
|
|
XR_001753740.2:n.2015T>A
|
|
|
NM_000455.5:c.1239T>A
MANE Select
|
NP_000446.1:p.Pro413=
|
|