|
ENST00000394867.9:n.974C>T
|
|
|
|
ENST00000687128.1:n.974C>T
|
|
|
|
ENST00000689792.1:n.475C>T
|
|
|
|
ENST00000262948.10:c.535C>T
MANE Select
|
ENSP00000262948.4:p.Arg179Trp
|
|
|
ENST00000262948.9:c.535C>T
|
ENSP00000262948.3:p.Arg179Trp
|
|
|
ENST00000394867.8:c.244C>T
|
ENSP00000378336.1:p.Arg82Trp
|
|
|
ENST00000593364.5:n.482C>T
|
|
|
|
ENST00000597008.5:n.136C>T
|
|
|
|
ENST00000599345.1:n.805C>T
|
|
|
|
ENST00000601786.5:n.836C>T
|
|
|
|
ENST00000602167.5:n.255C>T
|
|
|
|
NM_030662.3:c.535C>T , LRG_750t1:c.535C>T
|
NP_109587.1:p.Arg179Trp
|
|
|
XM_006722799.2:c.535C>T
|
XP_006722862.1:p.Arg179Trp
|
|
|
XM_011528133.1:c.-36C>T
|
XP_011526435.1:n.-36C>T
|
|
|
XM_017026989.1:c.535C>T
|
XP_016882478.1:p.Arg179Trp
|
|
|
XM_017026990.1:c.535C>T
|
XP_016882479.1:p.Arg179Trp
|
|
|
XM_017026991.1:c.535C>T
|
XP_016882480.1:p.Arg179Trp
|
|
|
NM_030662.4:c.535C>T
MANE Select
|
NP_109587.1:p.Arg179Trp
|
|
