ENST00000255078.8:c.1499A>T
MANE Select
|
ENSP00000255078.4:p.Glu500Val
|
|
ENST00000674955.1:c.*216A>T
|
ENSP00000502463.1:n.*216A>T
|
|
ENST00000675118.1:c.987A>T
|
|
|
ENST00000675205.1:n.183+394A>T
|
|
|
ENST00000675615.1:c.1499A>T
|
ENSP00000502413.1:p.Glu500Val
|
|
ENST00000675648.1:n.874A>T
|
|
|
ENST00000675997.1:n.113-589A>T
|
|
|
ENST00000676173.1:n.2244A>T
|
|
|
ENST00000676228.1:c.*822A>T
|
ENSP00000502375.1:n.*822A>T
|
|
ENST00000255078.7:c.1499A>T
|
ENSP00000255078.3:p.Glu500Val
|
|
ENST00000537458.5:n.616A>T
|
|
|
ENST00000539064.5:n.1258A>T
|
|
|
ENST00000541229.5:n.194A>T
|
|
|
ENST00000543739.5:n.616A>T
|
|
|
NM_002180.2:c.1499A>T , LRG_250t1:c.1499A>T
|
NP_002171.2:p.Glu500Val
|
|
XM_005273974.2:c.488A>T
|
XP_005274031.1:p.Glu163Val
|
|
XM_005273975.2:c.371A>T
|
XP_005274032.1:p.Glu124Val
|
|
XM_011544994.1:c.266A>T
|
XP_011543296.1:p.Glu89Val
|
|
XR_949903.1:n.1601A>T
|
|
|
XM_005273975.3:c.371A>T
|
XP_005274032.1:p.Glu124Val
|
|
XM_017017669.2:c.488A>T
|
XP_016873158.1:p.Glu163Val
|
|
XM_017017670.2:c.488A>T
|
XP_016873159.1:p.Glu163Val
|
|
XM_017017671.2:c.1499A>T
|
XP_016873160.1:p.Glu500Val
|
|
XR_949903.3:n.1597A>T
|
|
|
NM_002180.3:c.1499A>T
MANE Select
|
NP_002171.2:p.Glu500Val
|
|