ENST00000029410.10:c.375G>C
MANE Select
|
ENSP00000029410.5:p.Arg125=
|
|
ENST00000029410.9:c.375G>C
|
ENSP00000029410.5:p.Arg125=
|
|
ENST00000502420.1:n.354G>C
|
|
|
ENST00000505433.5:c.375G>C
|
ENSP00000425591.1:p.Arg125=
|
|
ENST00000505468.1:c.33G>C
|
ENSP00000420886.1:p.Arg11=
|
|
ENST00000507061.1:c.192G>C
|
ENSP00000423868.1:p.Arg64=
|
|
ENST00000510761.1:c.33G>C
|
ENSP00000423438.1:p.Arg11=
|
|
NM_007255.2:c.375G>C
|
NP_009186.1:p.Arg125=
|
|
XM_005265805.2:c.33G>C
|
XP_005265862.1:p.Arg11=
|
|
XM_006714816.2:c.-125G>C
|
XP_006714879.1:n.-125G>C
|
|
XM_011534421.1:c.33G>C
|
XP_011532723.1:p.Arg11=
|
|
XM_006714816.4:c.-125G>C
|
XP_006714879.1:n.-125G>C
|
|
XM_017008999.2:c.33G>C
|
XP_016864488.1:p.Arg11=
|
|
NM_007255.3:c.375G>C
MANE Select
|
NP_009186.1:p.Arg125=
|
|