ENST00000298139.7:c.3132G>C
MANE Select
|
ENSP00000298139.5:p.Thr1044=
|
|
ENST00000650667.1:c.*2746G>C
|
ENSP00000498593.1:n.*2746G>C
|
|
ENST00000298139.5:c.3132G>C
|
ENSP00000298139.5:p.Thr1044=
|
|
ENST00000521620.5:n.1765G>C
|
|
|
NM_000553.4:c.3132G>C , LRG_524t1:c.3132G>C
|
NP_000544.2:p.Thr1044=
|
|
XM_011544639.1:c.3051G>C
|
XP_011542941.1:p.Thr1017=
|
|
XM_011544640.1:c.1533G>C
|
XP_011542942.1:p.Thr511=
|
|
XR_949470.1:n.3405G>C
|
|
|
XR_949471.1:n.3405G>C
|
|
|
XR_949472.1:n.3405G>C
|
|
|
NM_000553.5:c.3132G>C
|
NP_000544.2:p.Thr1044=
|
|
XM_011544639.3:c.3051G>C
|
XP_011542941.1:p.Thr1017=
|
|
XM_024447265.1:c.2922G>C
|
XP_024303033.1:p.Thr974=
|
|
XR_949470.3:n.3433G>C
|
|
|
XR_949471.3:n.3433G>C
|
|
|
XR_949472.3:n.3433G>C
|
|
|
NM_000553.6:c.3132G>C
MANE Select
|
NP_000544.2:p.Thr1044=
|
|