ENST00000298139.7:c.3690A>G
MANE Select
|
ENSP00000298139.5:p.Thr1230=
|
|
ENST00000650667.1:c.*3304A>G
|
ENSP00000498593.1:n.*3304A>G
|
|
ENST00000298139.5:c.3690A>G
|
ENSP00000298139.5:p.Thr1230=
|
|
ENST00000521620.5:n.2323A>G
|
|
|
NM_000553.4:c.3690A>G , LRG_524t1:c.3690A>G
|
NP_000544.2:p.Thr1230=
|
|
XM_011544639.1:c.3609A>G
|
XP_011542941.1:p.Thr1203=
|
|
XM_011544640.1:c.2091A>G
|
XP_011542942.1:p.Thr697=
|
|
XR_949470.1:n.3963A>G
|
|
|
XR_949471.1:n.3963A>G
|
|
|
XR_949472.1:n.3963A>G
|
|
|
XR_949643.1:n.457-5961T>C
|
|
|
XR_949644.1:n.381-5961T>C
|
|
|
XR_949647.1:n.1070-5961T>C
|
|
|
XR_949648.1:n.972-5961T>C
|
|
|
NM_000553.5:c.3690A>G
|
NP_000544.2:p.Thr1230=
|
|
XM_011544639.3:c.3609A>G
|
XP_011542941.1:p.Thr1203=
|
|
XM_024447265.1:c.3480A>G
|
XP_024303033.1:p.Thr1160=
|
|
XR_949470.3:n.3991A>G
|
|
|
XR_949471.3:n.3991A>G
|
|
|
XR_949472.3:n.3991A>G
|
|
|
NM_000553.6:c.3690A>G
MANE Select
|
NP_000544.2:p.Thr1230=
|
|