ENST00000449291.7:c.1555-20C>T
MANE Select
|
ENSP00000401508.2:n.1555-20C>T
|
|
ENST00000340490.7:c.1620C>T
|
ENSP00000341136.3:p.Ser540=
|
|
ENST00000426292.7:c.1516-20C>T
|
ENSP00000390949.3:n.1516-20C>T
|
|
ENST00000435154.7:c.*244C>T
|
ENSP00000405670.3:n.*244C>T
|
|
ENST00000449291.6:c.1555-20C>T
|
ENSP00000401508.2:n.1555-20C>T
|
|
ENST00000460623.5:c.559C>T
|
|
|
ENST00000464332.5:n.1099-20C>T
|
|
|
ENST00000498076.5:n.334-20C>T
|
|
|
ENST00000529179.1:n.339-20C>T
|
|
|
NM_001286829.1:c.1516-20C>T
|
NP_001273758.1:n.1516-20C>T
|
|
NM_145201.5:c.1555-20C>T
|
NP_660202.3:n.1555-20C>T
|
|
XM_011517377.1:c.1292-20C>T
|
XP_011515679.1:n.1292-20C>T
|
|
NM_001363145.1:c.1474-20C>T
|
NP_001350074.1:n.1474-20C>T
|
|
NM_001363146.1:c.871-20C>T
|
NP_001350075.1:n.871-20C>T
|
|
XM_017013975.2:c.1839C>T
|
XP_016869464.1:p.Ser613=
|
|
XM_017013976.2:c.1774-20C>T
|
XP_016869465.1:n.1774-20C>T
|
|
XM_017013977.2:c.1539C>T
|
XP_016869466.1:p.Ser513=
|
|
XM_017013978.2:c.1511-20C>T
|
XP_016869467.1:n.1511-20C>T
|
|
XM_017013979.2:c.936C>T
|
XP_016869468.1:p.Ser312=
|
|
XM_024447332.1:c.929-20C>T
|
XP_024303100.1:n.929-20C>T
|
|
XM_024447333.1:c.855C>T
|
XP_024303101.1:p.Ser285=
|
|
NM_145201.6:c.1555-20C>T
MANE Select
|
NP_660202.3:n.1555-20C>T
|
|
NM_001286829.2:c.1516-20C>T
|
NP_001273758.1:n.1516-20C>T
|
|