ENST00000359206.8:c.3694C>T
|
ENSP00000352135.3:p.Arg1232Cys
|
|
ENST00000649586.2:c.3694C>T
MANE Select
|
ENSP00000496956.2:p.Arg1232Cys
|
|
ENST00000265723.8:c.3715C>T
|
ENSP00000265723.4:p.Arg1239Cys
|
|
ENST00000358400.7:c.3553C>T
|
ENSP00000351172.3:p.Arg1185Cys
|
|
ENST00000359206.7:c.3694C>T
|
ENSP00000352135.3:p.Arg1232Cys
|
|
ENST00000440025.1:c.128C>T
|
|
|
ENST00000453593.5:c.3553C>T
|
ENSP00000392983.1:p.Arg1185Cys
|
|
ENST00000467983.1:n.306C>T
|
|
|
NM_000443.3:c.3694C>T
|
NP_000434.1:p.Arg1232Cys
|
|
NM_018849.2:c.3715C>T
|
NP_061337.1:p.Arg1239Cys
|
|
NM_018850.2:c.3553C>T
|
NP_061338.1:p.Arg1185Cys
|
|
XM_011516308.1:c.3715C>T
|
XP_011514610.1:p.Arg1239Cys
|
|
XM_011516309.1:c.3694C>T
|
XP_011514611.1:p.Arg1232Cys
|
|
XM_011516310.1:c.3610C>T
|
XP_011514612.1:p.Arg1204Cys
|
|
XM_011516311.1:c.3586C>T
|
XP_011514613.1:p.Arg1196Cys
|
|
XM_011516312.1:c.3574C>T
|
XP_011514614.1:p.Arg1192Cys
|
|
XM_011516313.1:c.3553C>T
|
XP_011514615.1:p.Arg1185Cys
|
|
XM_011516314.1:c.3736C>T
|
XP_011514616.1:p.Arg1246Cys
|
|
XM_011516315.1:c.3055C>T
|
XP_011514617.1:p.Arg1019Cys
|
|
XM_011516308.3:c.3985C>T
|
XP_011514610.3:p.Arg1329Cys
|
|
XM_011516309.3:c.3964C>T
|
XP_011514611.3:p.Arg1322Cys
|
|
XM_011516310.3:c.3880C>T
|
XP_011514612.3:p.Arg1294Cys
|
|
XM_011516311.3:c.3856C>T
|
XP_011514613.3:p.Arg1286Cys
|
|
XM_011516312.3:c.3844C>T
|
XP_011514614.3:p.Arg1282Cys
|
|
XM_011516313.3:c.3823C>T
|
XP_011514615.2:p.Arg1275Cys
|
|
XM_011516315.3:c.3055C>T
|
XP_011514617.2:p.Arg1019Cys
|
|
XM_017012323.2:c.3715C>T
|
XP_016867812.1:p.Arg1239Cys
|
|
XR_001744809.2:n.4223C>T
|
|
|
NM_000443.4:c.3694C>T
MANE Select
|
NP_000434.1:p.Arg1232Cys
|
|
NM_018849.3:c.3715C>T
|
NP_061337.1:p.Arg1239Cys
|
|
NM_018850.3:c.3553C>T
|
NP_061338.1:p.Arg1185Cys
|
|