|
NM_006939.4:c.1720C>T
MANE Select
|
NP_008870.2:p.Arg574Cys
|
|
ENST00000216373.10:c.1720C>T
MANE Select
|
ENSP00000216373.5:p.Arg574Cys
|
|
NM_006939.2:c.1720C>T
|
NP_008870.2:p.Arg574Cys
|
|
NM_006939.3:c.1720C>T
|
NP_008870.2:p.Arg574Cys
|
|
ENST00000216373.9:c.1720C>T
|
ENSP00000216373.5:p.Arg574Cys
|
|
ENST00000543680.5:c.1621C>T
|
ENSP00000445328.1:p.Arg541Cys
|
|
ENST00000555794.2:c.834C>T
|
|
|
XM_005268021.1:c.1540C>T
|
XP_005268078.1:p.Arg514Cys
|
|
XM_011537103.1:c.1681C>T
|
XP_011535405.1:p.Arg561Cys
|
|
XM_011537104.1:c.1720C>T
|
XP_011535406.1:p.Arg574Cys
|