ENST00000317961.9:c.3680C>T
MANE Select
|
ENSP00000322408.4:p.Thr1227Ile
|
|
ENST00000317961.8:c.3680C>T
|
ENSP00000322408.4:p.Thr1227Ile
|
|
ENST00000382806.6:c.3509C>T
|
ENSP00000372256.2:p.Thr1170Ile
|
|
ENST00000415360.1:c.596C>T
|
ENSP00000389433.1:p.Thr199Ile
|
|
ENST00000440077.5:c.3557C>T
|
ENSP00000398543.1:p.Thr1186Ile
|
|
ENST00000469599.6:n.2278C>T
|
|
|
ENST00000492117.1:n.3572C>T
|
|
|
ENST00000541639.5:c.3773C>T
|
ENSP00000444293.1:p.Thr1258Ile
|
|
NM_001146705.1:c.3773C>T
|
NP_001140177.1:p.Thr1258Ile
|
|
NM_001146706.1:c.3509C>T
|
NP_001140178.1:p.Thr1170Ile
|
|
NM_004653.4:c.3680C>T
|
NP_004644.2:p.Thr1227Ile
|
|
XM_005262560.1:c.3545C>T
|
XP_005262617.1:p.Thr1182Ile
|
|
XM_005262561.1:c.3449C>T
|
XP_005262618.1:p.Thr1150Ile
|
|
XM_011531468.1:c.3602C>T
|
XP_011529770.1:p.Thr1201Ile
|
|
XR_244571.2:n.3968C>T
|
|
|
XR_430568.2:n.4302C>T
|
|
|
XM_005262560.3:c.3545C>T
|
XP_005262617.1:p.Thr1182Ile
|
|
XM_005262561.3:c.3449C>T
|
XP_005262618.1:p.Thr1150Ile
|
|
XM_011531468.3:c.3602C>T
|
XP_011529770.1:p.Thr1201Ile
|
|
XM_024452495.1:c.1670C>T
|
XP_024308263.1:p.Thr557Ile
|
|
XM_024452496.1:c.1436C>T
|
XP_024308264.1:p.Thr479Ile
|
|
XR_001756009.2:n.4418C>T
|
|
|
XR_001756010.2:n.4418C>T
|
|
|
XR_001756011.2:n.4283C>T
|
|
|
XR_001756012.2:n.4431C>T
|
|
|
XR_001756013.2:n.3749C>T
|
|
|
XR_002958832.1:n.3850C>T
|
|
|
XR_002958834.1:n.4074C>T
|
|
|
XR_002958835.1:n.3957C>T
|
|
|
XR_002958836.1:n.4640C>T
|
|
|
XR_002958837.1:n.4447C>T
|
|
|
XR_244571.4:n.3967C>T
|
|
|
XR_430568.4:n.4301C>T
|
|
|
NM_001146706.2:c.3509C>T
|
NP_001140178.1:p.Thr1170Ile
|
|
NM_004653.5:c.3680C>T
MANE Select
|
NP_004644.2:p.Thr1227Ile
|
|
NM_001146705.2:c.3773C>T
|
NP_001140177.1:p.Thr1258Ile
|
|