|
ENST00000560968.6:c.*104G=
|
ENSP00000453965.2:n.*104G=
|
|
|
ENST00000257555.11:c.1357G=
MANE Select
|
ENSP00000257555.5:p.Gly453=
|
|
|
ENST00000257555.10:c.1357G=
|
ENSP00000257555.4:p.Gly453=
|
|
|
ENST00000400024.6:c.1357G=
|
ENSP00000476181.1:p.Gly453=
|
|
|
ENST00000402929.5:n.2223G=
|
|
|
|
ENST00000535955.5:n.73G=
|
|
|
|
ENST00000538626.2:n.221G=
|
|
|
|
ENST00000538646.5:c.*333G=
|
ENSP00000443964.1:n.*333G=
|
|
|
ENST00000540108.1:c.*797G=
|
ENSP00000445445.1:n.*797G=
|
|
|
ENST00000541395.5:c.1357G=
|
ENSP00000443112.1:p.Gly453=
|
|
|
ENST00000541924.5:c.*371G=
|
ENSP00000440361.1:n.*371G=
|
|
|
ENST00000543255.1:n.401G=
|
|
|
|
ENST00000543427.5:c.820G=
|
ENSP00000439721.2:p.Gly274=
|
|
|
ENST00000544413.2:c.1357G=
|
ENSP00000438804.1:p.Gly453=
|
|
|
ENST00000544574.5:c.*120G=
|
ENSP00000438565.1:n.*120G=
|
|
|
ENST00000560968.5:c.1174G=
|
|
|
|
ENST00000615446.4:c.145G=
|
ENSP00000483994.1:p.Gly49=
|
|
|
ENST00000617366.4:c.587-113G=
|
ENSP00000481967.1:n.587-113G=
|
|
|
NM_000545.5:c.1357G= , LRG_522t1:c.1357G=
|
NP_000536.5:p.Gly453=
|
|
|
NM_000545.6:c.1357G=
|
NP_000536.5:p.Gly453=
|
|
|
NM_001306179.1:c.1357G=
|
NP_001293108.1:p.Gly453=
|
|
|
XM_005253931.2:c.1357G=
|
XP_005253988.1:p.Gly453=
|
|
|
XM_024449168.1:c.1357G=
|
XP_024304936.1:p.Gly453=
|
|
|
NM_000545.8:c.1357G=
MANE Select
|
NP_000536.6:p.Gly453=
|
|
|
NM_001306179.2:c.1357G=
|
NP_001293108.2:p.Gly453=
|
|
