ENST00000449291.7:c.1598G>C
MANE Select
|
ENSP00000401508.2:p.Cys533Ser
|
|
ENST00000340490.7:c.1683G>C
|
ENSP00000341136.3:p.Val561=
|
|
ENST00000426292.7:c.1559G>C
|
ENSP00000390949.3:p.Cys520Ser
|
|
ENST00000435154.7:c.*307G>C
|
ENSP00000405670.3:n.*307G>C
|
|
ENST00000449291.6:c.1598G>C
|
ENSP00000401508.2:p.Cys533Ser
|
|
ENST00000460623.5:c.622G>C
|
|
|
ENST00000464332.5:n.1142G>C
|
|
|
ENST00000498076.5:n.377G>C
|
|
|
ENST00000529179.1:n.382G>C
|
|
|
NM_001286829.1:c.1559G>C
|
NP_001273758.1:p.Cys520Ser
|
|
NM_145201.5:c.1598G>C
|
NP_660202.3:p.Cys533Ser
|
|
XM_011517377.1:c.1335G>C
|
XP_011515679.1:p.Val445=
|
|
NM_001363145.1:c.1517G>C
|
NP_001350074.1:p.Cys506Ser
|
|
NM_001363146.1:c.914G>C
|
NP_001350075.1:p.Cys305Ser
|
|
XM_017013975.2:c.1902G>C
|
XP_016869464.1:p.Val634=
|
|
XM_017013976.2:c.1817G>C
|
XP_016869465.1:p.Cys606Ser
|
|
XM_017013977.2:c.1602G>C
|
XP_016869466.1:p.Val534=
|
|
XM_017013978.2:c.1554G>C
|
XP_016869467.1:p.Val518=
|
|
XM_017013979.2:c.999G>C
|
XP_016869468.1:p.Val333=
|
|
XM_024447332.1:c.972G>C
|
XP_024303100.1:p.Val324=
|
|
XM_024447333.1:c.918G>C
|
XP_024303101.1:p.Val306=
|
|
NM_145201.6:c.1598G>C
MANE Select
|
NP_660202.3:p.Cys533Ser
|
|
NM_001286829.2:c.1559G>C
|
NP_001273758.1:p.Cys520Ser
|
|