ENST00000258385.8:c.1135A>C
MANE Select
|
ENSP00000258385.3:p.Ser379Arg
|
|
ENST00000258385.7:c.1135A>C
|
ENSP00000258385.3:p.Ser379Arg
|
|
ENST00000441621.6:c.*317A>C
|
ENSP00000408819.2:n.*317A>C
|
|
ENST00000446616.1:c.*776A>C
|
ENSP00000410801.1:n.*776A>C
|
|
ENST00000543200.5:c.1090A>C
|
ENSP00000438380.1:p.Ser364Arg
|
|
NM_000751.2:c.1135A>C
|
NP_000742.1:p.Ser379Arg
|
|
NM_001256657.1:c.1090A>C
|
NP_001243586.1:p.Ser364Arg
|
|
NM_001311195.1:c.553A>C
|
NP_001298124.1:p.Ser185Arg
|
|
NM_001311196.1:c.832A>C
|
NP_001298125.1:p.Ser278Arg
|
|
NR_046333.1:c.-4294966416A>C
|
|
|
NR_046334.1:c.-4294966137A>C
|
|
|
XM_011510524.1:c.754A>C
|
XP_011508826.1:p.Ser252Arg
|
|
XM_011510524.2:c.754A>C
|
XP_011508826.1:p.Ser252Arg
|
|
NM_000751.3:c.1135A>C
MANE Select
|
NP_000742.1:p.Ser379Arg
|
|
NM_001311195.2:c.553A>C
|
NP_001298124.1:p.Ser185Arg
|
|
NM_001311196.2:c.832A>C
|
NP_001298125.1:p.Ser278Arg
|
|
NM_001256657.2:c.1090A>C
|
NP_001243586.1:p.Ser364Arg
|
|