ENST00000260197.12:c.1494G>T
MANE Select
|
ENSP00000260197.6:p.Glu498Asp
|
|
ENST00000260197.11:c.1494G>T
|
ENSP00000260197.6:p.Glu498Asp
|
|
ENST00000532451.1:n.1446G>T
|
|
|
NM_003105.5:c.1494G>T
|
NP_003096.1:p.Glu498Asp
|
|
XM_011542963.1:c.1494G>T
|
XP_011541265.1:p.Glu498Asp
|
|
XM_011542964.1:c.1494G>T
|
XP_011541266.1:p.Glu498Asp
|
|
XM_011542965.1:c.-129G>T
|
XP_011541267.1:n.-129G>T
|
|
XM_011542963.3:c.1494G>T
|
XP_011541265.1:p.Glu498Asp
|
|
XM_011542965.3:c.-129G>T
|
XP_011541267.1:n.-129G>T
|
|
XM_017018169.2:c.1182G>T
|
XP_016873658.1:p.Glu394Asp
|
|
XM_017018170.2:c.969G>T
|
XP_016873659.1:p.Glu323Asp
|
|
XM_017018171.1:c.1494G>T
|
XP_016873660.1:p.Glu498Asp
|
|
NM_003105.6:c.1494G>T
MANE Select
|
NP_003096.2:p.Glu498Asp
|
|