ENST00000449291.7:c.1499C>A
MANE Select
|
ENSP00000401508.2:p.Ser500Tyr
|
|
ENST00000340490.7:c.1499C>A
|
ENSP00000341136.3:p.Ser500Tyr
|
|
ENST00000426292.7:c.1460C>A
|
ENSP00000390949.3:p.Ser487Tyr
|
|
ENST00000435154.7:c.*123C>A
|
ENSP00000405670.3:n.*123C>A
|
|
ENST00000449291.6:c.1499C>A
|
ENSP00000401508.2:p.Ser500Tyr
|
|
ENST00000460623.5:c.438C>A
|
|
|
ENST00000464332.5:n.1043C>A
|
|
|
ENST00000498076.5:n.278C>A
|
|
|
ENST00000529179.1:n.283C>A
|
|
|
NM_001286829.1:c.1460C>A
|
NP_001273758.1:p.Ser487Tyr
|
|
NM_145201.5:c.1499C>A
|
NP_660202.3:p.Ser500Tyr
|
|
XM_011517377.1:c.1292-141C>A
|
XP_011515679.1:n.1292-141C>A
|
|
NM_001363145.1:c.1418C>A
|
NP_001350074.1:p.Ser473Tyr
|
|
NM_001363146.1:c.815C>A
|
NP_001350075.1:p.Ser272Tyr
|
|
XM_017013975.2:c.1718C>A
|
XP_016869464.1:p.Ser573Tyr
|
|
XM_017013976.2:c.1718C>A
|
XP_016869465.1:p.Ser573Tyr
|
|
XM_017013977.2:c.1418C>A
|
XP_016869466.1:p.Ser473Tyr
|
|
XM_017013978.2:c.1511-141C>A
|
XP_016869467.1:n.1511-141C>A
|
|
XM_017013979.2:c.815C>A
|
XP_016869468.1:p.Ser272Tyr
|
|
XM_024447332.1:c.929-141C>A
|
XP_024303100.1:n.929-141C>A
|
|
XM_024447333.1:c.734C>A
|
XP_024303101.1:p.Ser245Tyr
|
|
NM_145201.6:c.1499C>A
MANE Select
|
NP_660202.3:p.Ser500Tyr
|
|
NM_001286829.2:c.1460C>A
|
NP_001273758.1:p.Ser487Tyr
|
|