|
ENST00000614091.5:c.-10G>T
|
ENSP00000482097.2:n.-10G>T
|
|
|
ENST00000623113.3:c.-10G>T
|
ENSP00000485413.2:n.-10G>T
|
|
|
ENST00000323670.14:c.-10G>T
MANE Select
|
ENSP00000313332.9:n.-10G>T
|
|
|
ENST00000323670.13:c.-10G>T
|
ENSP00000313332.8:n.-10G>T
|
|
|
ENST00000342680.5:c.-10G>T
|
ENSP00000345497.5:n.-10G>T
|
|
|
ENST00000392275.1:n.552-5446G>T
|
|
|
|
ENST00000392276.1:c.-32-5446G>T
|
ENSP00000376102.1:n.-32-5446G>T
|
|
|
ENST00000392278.2:c.24G>T
|
ENSP00000376103.2:p.Lys8Asn
|
|
|
ENST00000591243.1:c.-10G>T
|
ENSP00000467516.1:n.-10G>T
|
|
|
ENST00000592153.5:c.-10G>T
|
ENSP00000467117.1:n.-10G>T
|
|
|
ENST00000614091.4:c.-10G>T
|
ENSP00000482097.1:n.-10G>T
|
|
|
ENST00000623113.1:c.-32-5446G>T
|
ENSP00000485413.1:n.-32-5446G>T
|
|
|
NM_001031726.3:c.24G>T
|
NP_001026896.2:p.Lys8Asn
|
|
|
NM_001256046.1:c.-10G>T
|
NP_001242975.1:n.-10G>T
|
|
|
NM_001256047.1:c.-10G>T
|
NP_001242976.1:n.-10G>T
|
|
|
NM_001282929.1:c.-32-5446G>T
|
NP_001269858.1:n.-32-5446G>T
|
|
|
NM_001282930.1:c.-32-5446G>T
|
NP_001269859.1:n.-32-5446G>T
|
|
|
NM_001282931.1:c.-323G>T
|
NP_001269860.1:n.-323G>T
|
|
|
NM_031448.4:c.-10G>T
|
NP_113636.2:n.-10G>T
|
|
|
XM_024451734.1:c.153G>T
|
XP_024307502.1:p.Ser51=
|
|
|
XM_024451735.1:c.-10G>T
|
XP_024307503.1:n.-10G>T
|
|
|
XM_024451736.1:c.-10G>T
|
XP_024307504.1:n.-10G>T
|
|
|
XM_024451737.1:c.-10G>T
|
XP_024307505.1:n.-10G>T
|
|
|
XM_024451738.1:c.-10G>T
|
XP_024307506.1:n.-10G>T
|
|
|
NM_001256046.2:c.-10G>T
|
NP_001242975.1:n.-10G>T
|
|
|
NM_001282930.2:c.-32-5446G>T
|
NP_001269859.1:n.-32-5446G>T
|
|
|
NM_001282931.2:c.-323G>T
|
NP_001269860.1:n.-323G>T
|
|
|
NM_031448.6:c.-10G>T
MANE Select
|
NP_113636.2:n.-10G>T
|
|
|
NM_001031726.4:c.-10G>T
|
NP_001026896.3:n.-10G>T
|
|
|
NM_001256046.3:c.-10G>T
|
NP_001242975.1:n.-10G>T
|
|
|
NM_001256047.2:c.-10G>T
|
NP_001242976.1:n.-10G>T
|
|
|
NM_001282930.3:c.-32-5446G>T
|
NP_001269859.1:n.-32-5446G>T
|
|
|
NM_001282931.3:c.-323G>T
|
NP_001269860.1:n.-323G>T
|
|
