ENST00000456935.7:c.1056C>A
MANE Select
|
ENSP00000395473.2:p.Leu352=
|
|
ENST00000221363.8:c.1053C>A
|
ENSP00000221363.4:p.Leu351=
|
|
ENST00000456935.6:c.1056C>A
|
ENSP00000395473.2:p.Leu352=
|
|
ENST00000465830.1:n.137C>A
|
|
|
ENST00000466794.5:n.1009-137C>A
|
|
|
ENST00000495617.1:n.280+250C>A
|
|
|
NM_000528.3:c.1056C>A
|
NP_000519.2:p.Leu352=
|
|
NM_001173498.1:c.1053C>A
|
NP_001166969.1:p.Leu351=
|
|
XM_005259913.1:c.1059C>A
|
XP_005259970.1:p.Leu353=
|
|
XM_011528017.1:c.9-137C>A
|
XP_011526319.1:n.9-137C>A
|
|
XM_005259913.2:c.1059C>A
|
XP_005259970.1:p.Leu353=
|
|
XM_024451518.1:c.9-137C>A
|
XP_024307286.1:n.9-137C>A
|
|
NM_000528.4:c.1056C>A
MANE Select
|
NP_000519.2:p.Leu352=
|
|
NM_001173498.2:c.1053C>A
|
NP_001166969.1:p.Leu351=
|
|