|
NM_021939.4:c.1402C>T
MANE Select
|
NP_068758.3:p.Arg468Trp
|
|
ENST00000321562.9:c.1402C>T
MANE Select
|
ENSP00000317232.4:p.Arg468Trp
|
|
NM_021939.3:c.1402C>T , LRG_12t1:c.1402C>T
|
NP_068758.3:p.Arg468Trp
|
|
ENST00000321562.8:c.1402C>T
|
ENSP00000317232.4:p.Arg468Trp
|
|
ENST00000455106.1:c.813C>T
|
|
|
ENST00000464180.1:n.650C>T
|
|
|
ENST00000489591.5:c.*1186C>T
|
ENSP00000466352.1:n.*1186C>T
|
|
ENST00000490938.5:n.605C>T
|
|
|
ENST00000706683.1:c.1066C>T
|
ENSP00000516497.1:p.Arg356Trp
|
|
XM_011525099.1:c.1459C>T
|
XP_011523401.1:p.Arg487Trp
|
|
XM_011525099.3:c.1459C>T
|
XP_011523401.1:p.Arg487Trp
|
|
XM_011525100.1:c.1186C>T
|
XP_011523402.1:p.Arg396Trp
|
|
XM_011525100.2:c.1186C>T
|
XP_011523402.1:p.Arg396Trp
|