ENST00000439140.6:c.5255T>C
MANE Select
|
ENSP00000409937.1:p.Leu1752Ser
|
|
ENST00000286195.7:c.1664T>C
|
ENSP00000286195.3:p.Leu555Ser
|
|
ENST00000439140.5:c.5255T>C
|
ENSP00000409937.1:p.Leu1752Ser
|
|
ENST00000439802.5:c.*132T>C
|
ENSP00000400672.1:n.*132T>C
|
|
ENST00000482942.1:n.183T>C
|
|
|
NM_001168216.1:c.*132T>C
|
NP_001161688.1:n.*132T>C
|
|
NM_001168221.1:c.5255T>C
|
NP_001161693.1:p.Leu1752Ser
|
|
NM_152525.5:c.1664T>C
|
NP_689738.3:p.Leu555Ser
|
|
XM_005246347.2:c.5258T>C
|
XP_005246404.1:p.Leu1753Ser
|
|
XM_006712331.2:c.1667T>C
|
XP_006712394.1:p.Leu556Ser
|
|
XM_006712332.2:c.1592T>C
|
XP_006712395.1:p.Leu531Ser
|
|
XM_006712333.2:c.*132T>C
|
XP_006712396.1:n.*132T>C
|
|
XM_006712335.2:c.*69T>C
|
XP_006712398.1:n.*69T>C
|
|
XM_006712336.2:c.*69T>C
|
XP_006712399.1:n.*69T>C
|
|
XM_006712331.3:c.1667T>C
|
XP_006712394.1:p.Leu556Ser
|
|
XM_006712332.3:c.1592T>C
|
XP_006712395.1:p.Leu531Ser
|
|
XM_006712333.3:c.*132T>C
|
XP_006712396.1:n.*132T>C
|
|
XM_006712335.4:c.*69T>C
|
XP_006712398.1:n.*69T>C
|
|
XM_006712336.3:c.*69T>C
|
XP_006712399.1:n.*69T>C
|
|
XM_024452727.1:c.3620T>C
|
XP_024308495.1:p.Leu1207Ser
|
|
XM_024452728.1:c.1589T>C
|
XP_024308496.1:p.Leu530Ser
|
|
NM_001168221.2:c.5255T>C
MANE Select
|
NP_001161693.1:p.Leu1752Ser
|
|
NM_001168216.2:c.*132T>C
|
NP_001161688.1:n.*132T>C
|
|
NM_152525.6:c.1664T>C
|
NP_689738.3:p.Leu555Ser
|
|