ENST00000560968.6:c.*494C>T
|
ENSP00000453965.2:n.*494C>T
|
|
ENST00000257555.11:c.1747C>T
MANE Select
|
ENSP00000257555.5:p.Arg583Trp
|
|
ENST00000257555.10:c.1747C>T
|
ENSP00000257555.4:p.Arg583Trp
|
|
ENST00000540108.1:c.*1187C>T
|
ENSP00000445445.1:n.*1187C>T
|
|
ENST00000541395.5:c.1840C>T
|
ENSP00000443112.1:p.Arg614Trp
|
|
ENST00000543427.5:c.1210C>T
|
ENSP00000439721.2:p.Arg404Trp
|
|
ENST00000544413.2:c.1768C>T
|
ENSP00000438804.1:p.Arg590Trp
|
|
ENST00000560968.5:c.1564C>T
|
|
|
ENST00000615446.4:c.535C>T
|
ENSP00000483994.1:p.Arg179Trp
|
|
ENST00000617366.4:c.*156C>T
|
ENSP00000481967.1:n.*156C>T
|
|
NM_000545.5:c.1747C>T , LRG_522t1:c.1747C>T
|
NP_000536.5:p.Arg583Trp
|
|
NM_000545.6:c.1747C>T
|
NP_000536.5:p.Arg583Trp
|
|
NM_001306179.1:c.1768C>T
|
NP_001293108.1:p.Arg590Trp
|
|
XM_005253931.2:c.1840C>T
|
XP_005253988.1:p.Arg614Trp
|
|
XM_024449168.1:c.1840C>T
|
XP_024304936.1:p.Arg614Trp
|
|
NM_000545.8:c.1747C>T
MANE Select
|
NP_000536.6:p.Arg583Trp
|
|
NM_001306179.2:c.1768C>T
|
NP_001293108.2:p.Arg590Trp
|
|