|
NM_000459.5:c.2690A=
MANE Select
|
NP_000450.3:p.Tyr897=
|
|
ENST00000380036.10:c.2690A=
MANE Select
|
ENSP00000369375.4:p.Tyr897=
|
|
NM_000459.4:c.2690A=
|
NP_000450.2:p.Tyr897=
|
|
NM_001290077.1:c.2561A=
|
NP_001277006.1:p.Tyr854=
|
|
NM_001290078.1:c.2246A=
|
NP_001277007.1:p.Tyr749=
|
|
NM_001375475.1:c.2687A=
|
NP_001362404.1:p.Tyr896=
|
|
NM_001375476.1:c.2558A=
|
NP_001362405.1:p.Tyr853=
|
|
ENST00000380036.8:c.2690A=
|
ENSP00000369375.4:p.Tyr897=
|
|
ENST00000406359.8:c.2561A=
|
ENSP00000383977.4:p.Tyr854=
|
|
ENST00000519097.5:c.2246A=
|
ENSP00000430686.1:p.Tyr749=
|
|
ENST00000615002.4:c.*1191A=
|
ENSP00000480251.1:n.*1191A=
|
|
XM_005251561.1:c.2687A=
|
XP_005251618.1:p.Tyr896=
|
|
XM_005251561.2:c.2687A=
|
XP_005251618.1:p.Tyr896=
|
|
XM_005251563.1:c.2558A=
|
XP_005251620.1:p.Tyr853=
|
|
XM_005251563.2:c.2558A=
|
XP_005251620.1:p.Tyr853=
|