ENST00000317961.9:c.3299C>G
MANE Select
|
ENSP00000322408.4:p.Thr1100Ser
|
|
ENST00000317961.8:c.3299C>G
|
ENSP00000322408.4:p.Thr1100Ser
|
|
ENST00000382806.6:c.3128C>G
|
ENSP00000372256.2:p.Thr1043Ser
|
|
ENST00000415360.1:c.215C>G
|
ENSP00000389433.1:p.Thr72Ser
|
|
ENST00000440077.5:c.3176C>G
|
ENSP00000398543.1:p.Thr1059Ser
|
|
ENST00000469599.6:n.1897C>G
|
|
|
ENST00000492117.1:n.3191C>G
|
|
|
ENST00000541639.5:c.3392C>G
|
ENSP00000444293.1:p.Thr1131Ser
|
|
NM_001146705.1:c.3392C>G
|
NP_001140177.1:p.Thr1131Ser
|
|
NM_001146706.1:c.3128C>G
|
NP_001140178.1:p.Thr1043Ser
|
|
NM_004653.4:c.3299C>G
|
NP_004644.2:p.Thr1100Ser
|
|
XM_005262560.1:c.3164C>G
|
XP_005262617.1:p.Thr1055Ser
|
|
XM_005262561.1:c.3068C>G
|
XP_005262618.1:p.Thr1023Ser
|
|
XM_011531468.1:c.3221C>G
|
XP_011529770.1:p.Thr1074Ser
|
|
XR_244571.2:n.3587C>G
|
|
|
XR_430568.2:n.3921C>G
|
|
|
XM_005262560.3:c.3164C>G
|
XP_005262617.1:p.Thr1055Ser
|
|
XM_005262561.3:c.3068C>G
|
XP_005262618.1:p.Thr1023Ser
|
|
XM_011531468.3:c.3221C>G
|
XP_011529770.1:p.Thr1074Ser
|
|
XM_024452495.1:c.1289C>G
|
XP_024308263.1:p.Thr430Ser
|
|
XM_024452496.1:c.1055C>G
|
XP_024308264.1:p.Thr352Ser
|
|
XR_001756009.2:n.4037C>G
|
|
|
XR_001756010.2:n.4037C>G
|
|
|
XR_001756011.2:n.3902C>G
|
|
|
XR_001756012.2:n.4050C>G
|
|
|
XR_001756013.2:n.3368C>G
|
|
|
XR_002958832.1:n.3469C>G
|
|
|
XR_002958834.1:n.3693C>G
|
|
|
XR_002958835.1:n.3576C>G
|
|
|
XR_002958836.1:n.4259C>G
|
|
|
XR_002958837.1:n.4066C>G
|
|
|
XR_244571.4:n.3586C>G
|
|
|
XR_430568.4:n.3920C>G
|
|
|
NM_001146706.2:c.3128C>G
|
NP_001140178.1:p.Thr1043Ser
|
|
NM_004653.5:c.3299C>G
MANE Select
|
NP_004644.2:p.Thr1100Ser
|
|
NM_001146705.2:c.3392C>G
|
NP_001140177.1:p.Thr1131Ser
|
|