|
NM_022552.5:c.457C>T
MANE Select
|
NP_072046.2:p.Gln153Ter
|
|
ENST00000321117.10:c.457C>T
MANE Select
|
ENSP00000324375.5:p.Gln153Ter
|
|
NM_022552.4:c.457C>T , LRG_459t1:c.457C>T
|
NP_072046.2:p.Gln153Ter
|
|
NM_175629.2:c.457C>T , LRG_459t4:c.457C>T
|
NP_783328.1:p.Gln153Ter
|
|
NR_135490.1:n.795C>T
|
|
|
NR_135490.2:n.688C>T
|
|
|
ENST00000264709.7:c.457C>T
|
ENSP00000264709.3:p.Gln153Ter
|
|
ENST00000321117.9:c.457C>T
|
ENSP00000324375.5:p.Gln153Ter
|
|
ENST00000380756.7:c.457C>T
|
ENSP00000370132.3:p.Gln153Ter
|
|
XM_005264175.3:c.457C>T
|
XP_005264232.1:p.Gln153Ter
|
|
XM_005264175.5:c.457C>T
|
XP_005264232.1:p.Gln153Ter
|
|
XM_006711957.2:c.457C>T
|
XP_006712020.1:p.Gln153Ter
|
|
XM_006711958.2:c.13C>T
|
XP_006712021.1:p.Gln5Ter
|
|
XM_011532662.1:c.310C>T
|
XP_011530964.1:p.Gln104Ter
|
|
XM_011532662.2:c.310C>T
|
XP_011530964.1:p.Gln104Ter
|
|
XM_011532663.1:c.292C>T
|
XP_011530965.1:p.Gln98Ter
|
|
XM_011532663.2:c.292C>T
|
XP_011530965.1:p.Gln98Ter
|
|
XM_011532664.1:c.457C>T
|
XP_011530966.1:p.Gln153Ter
|
|
XM_011532664.2:c.457C>T
|
XP_011530966.1:p.Gln153Ter
|
|
XM_011532668.1:c.457C>T
|
XP_011530970.1:p.Gln153Ter
|
|
XM_017003526.1:c.457C>T
|
XP_016859015.1:p.Gln153Ter
|
|
XR_001738657.1:n.734C>T
|
|