ENST00000585465.3:c.*2844C>T
|
ENSP00000490268.2:n.*2844C>T
|
|
ENST00000585748.3:c.871C>T
|
ENSP00000477641.2:p.Arg291Cys
|
|
ENST00000585851.2:c.1069C>T
|
ENSP00000467912.2:p.Arg357Cys
|
|
ENST00000326873.12:c.1243C>T
MANE Select
|
ENSP00000324856.6:p.Arg415Cys
|
|
ENST00000326873.11:c.1243C>T
|
ENSP00000324856.6:p.Arg415Cys
|
|
ENST00000585465.2:n.2976C>T
|
|
|
ENST00000586243.5:c.1242C>T
|
ENSP00000467240.2:p.Pro414=
|
|
ENST00000589152.5:n.1941C>T
|
|
|
NM_000455.4:c.1243C>T , LRG_319t1:c.1243C>T
|
NP_000446.1:p.Arg415Cys
|
|
XM_005259617.1:c.1238C>T
|
XP_005259674.1:p.Pro413Leu
|
|
XM_011528209.1:c.1016C>T
|
XP_011526511.1:p.Pro339Leu
|
|
XM_005259617.3:c.1238C>T
|
XP_005259674.1:p.Pro413Leu
|
|
XM_011528209.2:c.1016C>T
|
XP_011526511.1:p.Pro339Leu
|
|
XR_001753738.2:n.2049C>T
|
|
|
XR_001753740.2:n.2019C>T
|
|
|
NM_000455.5:c.1243C>T
MANE Select
|
NP_000446.1:p.Arg415Cys
|
|