ENST00000391944.8:c.1891C>T
|
ENSP00000375808.4:p.Arg631Cys
|
|
ENST00000682414.1:c.1891C>T
|
ENSP00000507019.1:p.Arg631Cys
|
|
ENST00000682508.1:n.1920C>T
|
|
|
ENST00000684218.1:c.*1149C>T
|
ENSP00000507804.1:n.*1149C>T
|
|
ENST00000684264.1:n.1447C>T
|
|
|
ENST00000684407.1:c.1768C>T
|
ENSP00000507775.1:p.Arg590Cys
|
|
ENST00000684458.1:c.*377C>T
|
ENSP00000508260.1:n.*377C>T
|
|
ENST00000684468.1:n.1603C>T
|
|
|
ENST00000391945.10:c.1891C>T
MANE Select
|
ENSP00000375809.4:p.Arg631Cys
|
|
ENST00000646507.1:n.1988C>T
|
|
|
ENST00000391941.6:c.1819C>T
|
ENSP00000375805.2:p.Arg607Cys
|
|
ENST00000391942.6:n.1062C>T
|
|
|
ENST00000391944.7:c.1657C>T
|
ENSP00000375808.3:p.Arg553Cys
|
|
ENST00000391945.8:c.1891C>T
|
ENSP00000375809.3:p.Arg631Cys
|
|
ENST00000588652.5:n.1979C>T
|
|
|
NM_000400.3:c.1891C>T , LRG_461t1:c.1891C>T
|
NP_000391.1:p.Arg631Cys
|
|
XM_011526611.1:c.1813C>T
|
XP_011524913.1:p.Arg605Cys
|
|
XM_011526611.2:c.1813C>T
|
XP_011524913.1:p.Arg605Cys
|
|
XM_017026467.1:c.1768C>T
|
XP_016881956.1:p.Arg590Cys
|
|
XR_001753633.2:n.1938C>T
|
|
|
XR_001753634.2:n.1874C>T
|
|
|
NM_000400.4:c.1891C>T
MANE Select
|
NP_000391.1:p.Arg631Cys
|
|