ENST00000380036.10:c.2697C>T
MANE Select
|
ENSP00000369375.4:p.Tyr899=
|
|
ENST00000380036.8:c.2697C>T
|
ENSP00000369375.4:p.Tyr899=
|
|
ENST00000406359.8:c.2568C>T
|
ENSP00000383977.4:p.Tyr856=
|
|
ENST00000519097.5:c.2253C>T
|
ENSP00000430686.1:p.Tyr751=
|
|
ENST00000615002.4:c.*1198C>T
|
ENSP00000480251.1:n.*1198C>T
|
|
NM_000459.4:c.2697C>T
|
NP_000450.2:p.Tyr899=
|
|
NM_001290077.1:c.2568C>T
|
NP_001277006.1:p.Tyr856=
|
|
NM_001290078.1:c.2253C>T
|
NP_001277007.1:p.Tyr751=
|
|
XM_005251561.1:c.2694C>T
|
XP_005251618.1:p.Tyr898=
|
|
XM_005251563.1:c.2565C>T
|
XP_005251620.1:p.Tyr855=
|
|
XM_005251561.2:c.2694C>T
|
XP_005251618.1:p.Tyr898=
|
|
XM_005251563.2:c.2565C>T
|
XP_005251620.1:p.Tyr855=
|
|
NM_000459.5:c.2697C>T
MANE Select
|
NP_000450.3:p.Tyr899=
|
|
NM_001375475.1:c.2694C>T
|
NP_001362404.1:p.Tyr898=
|
|
NM_001375476.1:c.2565C>T
|
NP_001362405.1:p.Tyr855=
|
|