ENST00000029410.10:c.351C>G
MANE Select
|
ENSP00000029410.5:p.Arg117=
|
|
ENST00000029410.9:c.351C>G
|
ENSP00000029410.5:p.Arg117=
|
|
ENST00000502420.1:n.330C>G
|
|
|
ENST00000505433.5:c.351C>G
|
ENSP00000425591.1:p.Arg117=
|
|
ENST00000505468.1:c.9C>G
|
ENSP00000420886.1:p.Arg3=
|
|
ENST00000507061.1:c.168C>G
|
ENSP00000423868.1:p.Arg56=
|
|
ENST00000510761.1:c.9C>G
|
ENSP00000423438.1:p.Arg3=
|
|
NM_007255.2:c.351C>G
|
NP_009186.1:p.Arg117=
|
|
XM_005265805.2:c.9C>G
|
XP_005265862.1:p.Arg3=
|
|
XM_006714816.2:c.-149C>G
|
XP_006714879.1:n.-149C>G
|
|
XM_011534421.1:c.9C>G
|
XP_011532723.1:p.Arg3=
|
|
XM_006714816.4:c.-149C>G
|
XP_006714879.1:n.-149C>G
|
|
XM_017008999.2:c.9C>G
|
XP_016864488.1:p.Arg3=
|
|
NM_007255.3:c.351C>G
MANE Select
|
NP_009186.1:p.Arg117=
|
|