ENST00000317961.9:c.3319G>T
MANE Select
|
ENSP00000322408.4:p.Glu1107Ter
|
|
ENST00000317961.8:c.3319G>T
|
ENSP00000322408.4:p.Glu1107Ter
|
|
ENST00000382806.6:c.3148G>T
|
ENSP00000372256.2:p.Glu1050Ter
|
|
ENST00000415360.1:c.235G>T
|
ENSP00000389433.1:p.Glu79Ter
|
|
ENST00000440077.5:c.3196G>T
|
ENSP00000398543.1:p.Glu1066Ter
|
|
ENST00000469599.6:n.1917G>T
|
|
|
ENST00000492117.1:n.3211G>T
|
|
|
ENST00000541639.5:c.3412G>T
|
ENSP00000444293.1:p.Glu1138Ter
|
|
NM_001146705.1:c.3412G>T
|
NP_001140177.1:p.Glu1138Ter
|
|
NM_001146706.1:c.3148G>T
|
NP_001140178.1:p.Glu1050Ter
|
|
NM_004653.4:c.3319G>T
|
NP_004644.2:p.Glu1107Ter
|
|
XM_005262560.1:c.3184G>T
|
XP_005262617.1:p.Glu1062Ter
|
|
XM_005262561.1:c.3088G>T
|
XP_005262618.1:p.Glu1030Ter
|
|
XM_011531468.1:c.3241G>T
|
XP_011529770.1:p.Glu1081Ter
|
|
XR_244571.2:n.3607G>T
|
|
|
XR_430568.2:n.3941G>T
|
|
|
XM_005262560.3:c.3184G>T
|
XP_005262617.1:p.Glu1062Ter
|
|
XM_005262561.3:c.3088G>T
|
XP_005262618.1:p.Glu1030Ter
|
|
XM_011531468.3:c.3241G>T
|
XP_011529770.1:p.Glu1081Ter
|
|
XM_024452495.1:c.1309G>T
|
XP_024308263.1:p.Glu437Ter
|
|
XM_024452496.1:c.1075G>T
|
XP_024308264.1:p.Glu359Ter
|
|
XR_001756009.2:n.4057G>T
|
|
|
XR_001756010.2:n.4057G>T
|
|
|
XR_001756011.2:n.3922G>T
|
|
|
XR_001756012.2:n.4070G>T
|
|
|
XR_001756013.2:n.3388G>T
|
|
|
XR_002958832.1:n.3489G>T
|
|
|
XR_002958834.1:n.3713G>T
|
|
|
XR_002958835.1:n.3596G>T
|
|
|
XR_002958836.1:n.4279G>T
|
|
|
XR_002958837.1:n.4086G>T
|
|
|
XR_244571.4:n.3606G>T
|
|
|
XR_430568.4:n.3940G>T
|
|
|
NM_001146706.2:c.3148G>T
|
NP_001140178.1:p.Glu1050Ter
|
|
NM_004653.5:c.3319G>T
MANE Select
|
NP_004644.2:p.Glu1107Ter
|
|
NM_001146705.2:c.3412G>T
|
NP_001140177.1:p.Glu1138Ter
|
|