ENST00000598261.2:c.193A>G
|
ENSP00000469798.1:p.Ser65Gly
|
|
ENST00000598742.6:c.180A>G
MANE Select
|
ENSP00000470972.1:p.Thr60=
|
|
ENST00000600467.6:c.180A>G
|
ENSP00000469228.2:p.Thr60=
|
|
ENST00000221975.6:c.-43A>G
|
ENSP00000221975.2:n.-43A>G
|
|
ENST00000593863.5:c.180A>G
|
ENSP00000470004.1:p.Thr60=
|
|
ENST00000598261.1:c.193A>G
|
ENSP00000469798.1:p.Ser65Gly
|
|
ENST00000598399.1:c.1018A>G
|
ENSP00000472660.1:n.1018A>G
|
|
ENST00000598742.5:c.180A>G
|
ENSP00000470972.1:p.Thr60=
|
|
ENST00000600467.5:c.180A>G
|
ENSP00000469228.1:p.Thr60=
|
|
ENST00000601492.5:c.261A>G
|
ENSP00000471621.1:p.Thr87=
|
|
NM_001022.3:c.180A>G
|
NP_001013.1:p.Thr60=
|
|
NM_001321483.1:c.180A>G
|
NP_001308412.1:p.Thr60=
|
|
NM_001321484.1:c.180A>G
|
NP_001308413.1:p.Thr60=
|
|
NM_001321485.1:c.193A>G
|
NP_001308414.1:p.Ser65Gly
|
|
XM_017027113.2:c.180A>G
|
XP_016882602.1:p.Thr60=
|
|
NM_001022.4:c.180A>G
MANE Select
|
NP_001013.1:p.Thr60=
|
|
NM_001321483.2:c.180A>G
|
NP_001308412.1:p.Thr60=
|
|
NM_001321484.2:c.180A>G
|
NP_001308413.1:p.Thr60=
|
|
NM_001321485.2:c.193A>G
|
NP_001308414.1:p.Ser65Gly
|
|