|
NM_001079537.2:c.124C>T
MANE Select
|
NP_001073005.1:p.Arg42Ter
|
|
ENST00000330149.10:c.124C>T
MANE Select
|
ENSP00000330289.5:p.Arg42Ter
|
|
NM_001079537.1:c.124C>T
|
NP_001073005.1:p.Arg42Ter
|
|
NM_177452.3:c.124C>T
|
NP_803235.1:p.Arg42Ter
|
|
NM_177452.4:c.124C>T
|
NP_803235.1:p.Arg42Ter
|
|
ENST00000330149.9:c.124C>T
|
ENSP00000330289.5:p.Arg42Ter
|
|
ENST00000347691.9:c.124C>T
|
ENSP00000335171.6:p.Arg42Ter
|
|
ENST00000469361.5:n.561C>T
|
|
|
ENST00000554018.1:c.121C>T
|
ENSP00000450670.1:p.Arg41Ter
|
|
ENST00000555269.5:c.124C>T
|
ENSP00000452236.1:p.Arg42Ter
|
|
ENST00000556765.1:c.124C>T
|
ENSP00000451711.1:p.Arg42Ter
|
|
ENST00000557764.5:n.301-5214C>T
|
|
|
XM_011536409.1:c.10C>T
|
XP_011534711.1:p.Arg4Ter
|
|
XM_011536409.2:c.10C>T
|
XP_011534711.1:p.Arg4Ter
|
|
XM_017020964.2:c.124C>T
|
XP_016876453.1:p.Arg42Ter
|