|
NM_001235.5:c.1119C>T
MANE Select
|
NP_001226.2:p.Arg373=
|
|
ENST00000358171.8:c.1119C>T
MANE Select
|
ENSP00000350894.4:p.Arg373=
|
|
NM_001207014.1:c.1119C>T
|
NP_001193943.1:p.Arg373=
|
|
NM_001207014.2:c.1119C>T
|
NP_001193943.1:p.Arg373=
|
|
NM_001207014.3:c.1119C>T
|
NP_001193943.1:p.Arg373=
|
|
NM_001235.3:c.1119C>T
|
NP_001226.2:p.Arg373=
|
|
ENST00000358171.7:c.1119C>T
|
ENSP00000350894.3:p.Arg373=
|
|
ENST00000524558.5:c.1119C>T
|
ENSP00000434412.1:p.Arg373=
|
|
ENST00000525876.1:c.468C>T
|
ENSP00000433532.1:p.Arg156=
|
|
ENST00000526638.1:c.32C>T
|
|
|
ENST00000533603.5:c.1119C>T
|
ENSP00000434657.1:p.Arg373=
|
|
ENST00000649490.1:c.*1770C>T
|
ENSP00000497544.1:n.*1770C>T
|
|
XM_006718729.1:c.1119C>T
|
XP_006718792.1:p.Arg373=
|
|
XM_011545326.1:c.1119C>T
|
XP_011543628.1:p.Arg373=
|
|
XM_011545327.1:c.1119C>T
|
XP_011543629.1:p.Arg373=
|
|
XM_024448756.1:c.1119C>T
|
XP_024304524.1:p.Arg373=
|