ENST00000317961.9:c.3387C>G
MANE Select
|
ENSP00000322408.4:p.Asp1129Glu
|
|
ENST00000317961.8:c.3387C>G
|
ENSP00000322408.4:p.Asp1129Glu
|
|
ENST00000382806.6:c.3216C>G
|
ENSP00000372256.2:p.Asp1072Glu
|
|
ENST00000415360.1:c.303C>G
|
ENSP00000389433.1:p.Asp101Glu
|
|
ENST00000440077.5:c.3264C>G
|
ENSP00000398543.1:p.Asp1088Glu
|
|
ENST00000469599.6:n.1985C>G
|
|
|
ENST00000492117.1:n.3279C>G
|
|
|
ENST00000541639.5:c.3480C>G
|
ENSP00000444293.1:p.Asp1160Glu
|
|
NM_001146705.1:c.3480C>G
|
NP_001140177.1:p.Asp1160Glu
|
|
NM_001146706.1:c.3216C>G
|
NP_001140178.1:p.Asp1072Glu
|
|
NM_004653.4:c.3387C>G
|
NP_004644.2:p.Asp1129Glu
|
|
XM_005262560.1:c.3252C>G
|
XP_005262617.1:p.Asp1084Glu
|
|
XM_005262561.1:c.3156C>G
|
XP_005262618.1:p.Asp1052Glu
|
|
XM_011531468.1:c.3309C>G
|
XP_011529770.1:p.Asp1103Glu
|
|
XR_244571.2:n.3675C>G
|
|
|
XR_430568.2:n.4009C>G
|
|
|
XM_005262560.3:c.3252C>G
|
XP_005262617.1:p.Asp1084Glu
|
|
XM_005262561.3:c.3156C>G
|
XP_005262618.1:p.Asp1052Glu
|
|
XM_011531468.3:c.3309C>G
|
XP_011529770.1:p.Asp1103Glu
|
|
XM_024452495.1:c.1377C>G
|
XP_024308263.1:p.Asp459Glu
|
|
XM_024452496.1:c.1143C>G
|
XP_024308264.1:p.Asp381Glu
|
|
XR_001756009.2:n.4125C>G
|
|
|
XR_001756010.2:n.4125C>G
|
|
|
XR_001756011.2:n.3990C>G
|
|
|
XR_001756012.2:n.4138C>G
|
|
|
XR_001756013.2:n.3456C>G
|
|
|
XR_002958832.1:n.3557C>G
|
|
|
XR_002958834.1:n.3781C>G
|
|
|
XR_002958835.1:n.3664C>G
|
|
|
XR_002958836.1:n.4347C>G
|
|
|
XR_002958837.1:n.4154C>G
|
|
|
XR_244571.4:n.3674C>G
|
|
|
XR_430568.4:n.4008C>G
|
|
|
NM_001146706.2:c.3216C>G
|
NP_001140178.1:p.Asp1072Glu
|
|
NM_004653.5:c.3387C>G
MANE Select
|
NP_004644.2:p.Asp1129Glu
|
|
NM_001146705.2:c.3480C>G
|
NP_001140177.1:p.Asp1160Glu
|
|