ENST00000449291.7:c.1594C>A
MANE Select
|
ENSP00000401508.2:p.Leu532Met
|
|
ENST00000340490.7:c.1679C>A
|
ENSP00000341136.3:p.Ser560Tyr
|
|
ENST00000426292.7:c.1555C>A
|
ENSP00000390949.3:p.Leu519Met
|
|
ENST00000435154.7:c.*303C>A
|
ENSP00000405670.3:n.*303C>A
|
|
ENST00000449291.6:c.1594C>A
|
ENSP00000401508.2:p.Leu532Met
|
|
ENST00000460623.5:c.618C>A
|
|
|
ENST00000464332.5:n.1138C>A
|
|
|
ENST00000498076.5:n.373C>A
|
|
|
ENST00000529179.1:n.378C>A
|
|
|
NM_001286829.1:c.1555C>A
|
NP_001273758.1:p.Leu519Met
|
|
NM_145201.5:c.1594C>A
|
NP_660202.3:p.Leu532Met
|
|
XM_011517377.1:c.1331C>A
|
XP_011515679.1:p.Ser444Tyr
|
|
NM_001363145.1:c.1513C>A
|
NP_001350074.1:p.Leu505Met
|
|
NM_001363146.1:c.910C>A
|
NP_001350075.1:p.Leu304Met
|
|
XM_017013975.2:c.1898C>A
|
XP_016869464.1:p.Ser633Tyr
|
|
XM_017013976.2:c.1813C>A
|
XP_016869465.1:p.Leu605Met
|
|
XM_017013977.2:c.1598C>A
|
XP_016869466.1:p.Ser533Tyr
|
|
XM_017013978.2:c.1550C>A
|
XP_016869467.1:p.Ser517Tyr
|
|
XM_017013979.2:c.995C>A
|
XP_016869468.1:p.Ser332Tyr
|
|
XM_024447332.1:c.968C>A
|
XP_024303100.1:p.Ser323Tyr
|
|
XM_024447333.1:c.914C>A
|
XP_024303101.1:p.Ser305Tyr
|
|
NM_145201.6:c.1594C>A
MANE Select
|
NP_660202.3:p.Leu532Met
|
|
NM_001286829.2:c.1555C>A
|
NP_001273758.1:p.Leu519Met
|
|