ENST00000456935.7:c.2911A=
MANE Select
|
ENSP00000395473.2:p.Thr971=
|
|
ENST00000221363.8:c.2908A=
|
ENSP00000221363.4:p.Thr970=
|
|
ENST00000456935.6:c.2911A=
|
ENSP00000395473.2:p.Thr971=
|
|
ENST00000466794.5:n.3501A=
|
|
|
ENST00000469423.1:n.340A=
|
|
|
ENST00000493218.5:n.322A=
|
|
|
ENST00000597692.1:c.470A=
|
|
|
NM_000528.3:c.2911A=
|
NP_000519.2:p.Thr971=
|
|
NM_001173498.1:c.2908A=
|
NP_001166969.1:p.Thr970=
|
|
XM_005259913.1:c.2914A=
|
XP_005259970.1:p.Thr972=
|
|
XM_011528017.1:c.1810A=
|
XP_011526319.1:p.Thr604=
|
|
XM_005259913.2:c.2914A=
|
XP_005259970.1:p.Thr972=
|
|
XM_024451518.1:c.1810A=
|
XP_024307286.1:p.Thr604=
|
|
NM_000528.4:c.2911A=
MANE Select
|
NP_000519.2:p.Thr971=
|
|
NM_001173498.2:c.2908A=
|
NP_001166969.1:p.Thr970=
|
|