ENST00000576204.6:n.815G=
|
|
|
ENST00000622290.5:c.*124G=
|
ENSP00000483331.2:n.*124G=
|
|
ENST00000205557.12:c.3952G=
MANE Select
|
ENSP00000205557.7:p.Ala1318=
|
|
ENST00000640696.1:c.766G=
|
ENSP00000492197.1:p.Ala256=
|
|
ENST00000205557.11:c.3952G=
|
ENSP00000205557.7:p.Ala1318=
|
|
ENST00000456970.6:c.3577G=
|
ENSP00000405002.2:n.3577G=
|
|
ENST00000576204.5:n.815G=
|
|
|
ENST00000622290.4:c.*1161G=
|
ENSP00000483331.1:n.*1161G=
|
|
NM_001171.5:c.3952G=
|
NP_001162.4:p.Ala1318=
|
|
XM_011522479.1:c.3919G=
|
XP_011520781.1:p.Ala1307=
|
|
XM_011522480.1:c.3610G=
|
XP_011520782.1:p.Ala1204=
|
|
XM_011522481.1:c.3610G=
|
XP_011520783.1:p.Ala1204=
|
|
XR_932836.1:n.4250G=
|
|
|
XR_932837.1:n.3988G=
|
|
|
XR_932838.1:n.4051G=
|
|
|
XR_933134.1:n.539-4819C=
|
|
|
NM_001351800.1:c.3610G=
|
NP_001338729.1:p.Ala1204=
|
|
NR_147784.1:n.3614G=
|
|
|
XM_011522479.2:c.3919G=
|
XP_011520781.1:p.Ala1307=
|
|
XM_011522481.3:c.3610G=
|
XP_011520783.1:p.Ala1204=
|
|
XM_017023212.1:c.3784G=
|
XP_016878701.1:p.Ala1262=
|
|
XM_024450261.1:c.3988G=
|
XP_024306029.1:p.Ala1330=
|
|
XR_932837.3:n.3933G=
|
|
|
NM_001171.6:c.3952G=
MANE Select
|
NP_001162.5:p.Ala1318=
|
|