ENST00000684745.1:n.994G>C
|
|
|
ENST00000379374.5:c.1320G>C
MANE Select
|
ENSP00000368682.4:p.Glu440Asp
|
|
ENST00000379374.4:c.1320G>C
|
ENSP00000368682.4:p.Glu440Asp
|
|
NM_000444.5:c.1320G>C
|
NP_000435.3:p.Glu440Asp
|
|
NM_001282754.1:c.1320G>C
|
NP_001269683.1:p.Glu440Asp
|
|
XM_011545533.1:c.564G>C
|
XP_011543835.1:p.Glu188Asp
|
|
XM_011545534.1:c.564G>C
|
XP_011543836.1:p.Glu188Asp
|
|
XM_011545535.1:c.1320G>C
|
XP_011543837.1:p.Glu440Asp
|
|
XM_011545536.1:c.213G>C
|
XP_011543838.1:p.Glu71Asp
|
|
XM_011545536.2:c.213G>C
|
XP_011543838.1:p.Glu71Asp
|
|
XM_017029579.1:c.564G>C
|
XP_016885068.1:p.Glu188Asp
|
|
XM_024452390.1:c.1029G>C
|
XP_024308158.1:p.Glu343Asp
|
|
XR_001755695.1:n.1999G>C
|
|
|
NM_000444.6:c.1320G>C
MANE Select
|
NP_000435.3:p.Glu440Asp
|
|
NM_001282754.2:c.1320G>C
|
NP_001269683.1:p.Glu440Asp
|
|