|
ENST00000560968.6:c.597G>C
|
ENSP00000453965.2:p.Gly199=
|
|
|
ENST00000257555.11:c.597G>C
MANE Select
|
ENSP00000257555.5:p.Gly199=
|
|
|
ENST00000257555.10:c.597G>C
|
ENSP00000257555.4:p.Gly199=
|
|
|
ENST00000400024.6:c.597G>C
|
ENSP00000476181.1:p.Gly199=
|
|
|
ENST00000402929.5:n.732G>C
|
|
|
|
ENST00000535955.5:n.43-3901G>C
|
|
|
|
ENST00000538626.2:n.191-3901G>C
|
|
|
|
ENST00000538646.5:c.527-574G>C
|
ENSP00000443964.1:n.527-574G>C
|
|
|
ENST00000540108.1:c.*37G>C
|
ENSP00000445445.1:n.*37G>C
|
|
|
ENST00000541395.5:c.597G>C
|
ENSP00000443112.1:p.Gly199=
|
|
|
ENST00000541924.5:c.597G>C
|
ENSP00000440361.1:p.Gly199=
|
|
|
ENST00000543427.5:c.597G>C
|
ENSP00000439721.2:p.Gly199=
|
|
|
ENST00000544413.2:c.597G>C
|
ENSP00000438804.1:p.Gly199=
|
|
|
ENST00000544574.5:c.73-3027G>C
|
ENSP00000438565.1:n.73-3027G>C
|
|
|
ENST00000560968.5:c.740G>C
|
|
|
|
ENST00000615446.4:c.-257-2672G>C
|
ENSP00000483994.1:n.-257-2672G>C
|
|
|
ENST00000617366.4:c.586+11G>C
|
ENSP00000481967.1:n.586+11G>C
|
|
|
NM_000545.5:c.597G>C , LRG_522t1:c.597G>C
|
NP_000536.5:p.Gly199=
|
|
|
NM_000545.6:c.597G>C
|
NP_000536.5:p.Gly199=
|
|
|
NM_001306179.1:c.597G>C
|
NP_001293108.1:p.Gly199=
|
|
|
XM_005253931.2:c.597G>C
|
XP_005253988.1:p.Gly199=
|
|
|
XM_024449168.1:c.597G>C
|
XP_024304936.1:p.Gly199=
|
|
|
NM_000545.8:c.597G>C
MANE Select
|
NP_000536.6:p.Gly199=
|
|
|
NM_001306179.2:c.597G>C
|
NP_001293108.2:p.Gly199=
|
|
