ENST00000449291.7:c.1592G>C
MANE Select
|
ENSP00000401508.2:p.Ser531Thr
|
|
ENST00000340490.7:c.1677G>C
|
ENSP00000341136.3:p.Gln559His
|
|
ENST00000426292.7:c.1553G>C
|
ENSP00000390949.3:p.Ser518Thr
|
|
ENST00000435154.7:c.*301G>C
|
ENSP00000405670.3:n.*301G>C
|
|
ENST00000449291.6:c.1592G>C
|
ENSP00000401508.2:p.Ser531Thr
|
|
ENST00000460623.5:c.616G>C
|
|
|
ENST00000464332.5:n.1136G>C
|
|
|
ENST00000498076.5:n.371G>C
|
|
|
ENST00000529179.1:n.376G>C
|
|
|
NM_001286829.1:c.1553G>C
|
NP_001273758.1:p.Ser518Thr
|
|
NM_145201.5:c.1592G>C
|
NP_660202.3:p.Ser531Thr
|
|
XM_011517377.1:c.1329G>C
|
XP_011515679.1:p.Gln443His
|
|
NM_001363145.1:c.1511G>C
|
NP_001350074.1:p.Ser504Thr
|
|
NM_001363146.1:c.908G>C
|
NP_001350075.1:p.Ser303Thr
|
|
XM_017013975.2:c.1896G>C
|
XP_016869464.1:p.Gln632His
|
|
XM_017013976.2:c.1811G>C
|
XP_016869465.1:p.Ser604Thr
|
|
XM_017013977.2:c.1596G>C
|
XP_016869466.1:p.Gln532His
|
|
XM_017013978.2:c.1548G>C
|
XP_016869467.1:p.Gln516His
|
|
XM_017013979.2:c.993G>C
|
XP_016869468.1:p.Gln331His
|
|
XM_024447332.1:c.966G>C
|
XP_024303100.1:p.Gln322His
|
|
XM_024447333.1:c.912G>C
|
XP_024303101.1:p.Gln304His
|
|
NM_145201.6:c.1592G>C
MANE Select
|
NP_660202.3:p.Ser531Thr
|
|
NM_001286829.2:c.1553G>C
|
NP_001273758.1:p.Ser518Thr
|
|