ENST00000373547.9:c.790C>T
MANE Select
|
ENSP00000362648.4:p.Arg264Cys
|
|
ENST00000373547.8:c.790C>T
|
ENSP00000362648.4:p.Arg264Cys
|
|
ENST00000415905.5:c.724C>T
|
ENSP00000411744.1:p.Arg242Cys
|
|
ENST00000451402.5:c.901C>T
|
ENSP00000392147.1:p.Arg301Cys
|
|
NM_001123355.1:c.901C>T
|
NP_001116827.1:p.Arg301Cys
|
|
NM_001123369.1:c.724C>T
|
NP_001116841.1:p.Arg242Cys
|
|
NM_002721.4:c.790C>T
|
NP_002712.1:p.Arg264Cys
|
|
XM_011518847.1:c.754C>T
|
XP_011517149.1:p.Arg252Cys
|
|
XM_011518847.3:c.754C>T
|
XP_011517149.1:p.Arg252Cys
|
|
XM_024447607.1:c.349C>T
|
XP_024303375.1:p.Arg117Cys
|
|
NM_002721.5:c.790C>T
MANE Select
|
NP_002712.1:p.Arg264Cys
|
|
NM_001123355.2:c.901C>T
|
NP_001116827.1:p.Arg301Cys
|
|
NM_001123369.2:c.724C>T
|
NP_001116841.1:p.Arg242Cys
|
|