ENST00000181839.10:c.2063G>A
MANE Select
|
ENSP00000181839.4:p.Gly688Asp
|
|
ENST00000340829.10:c.2063G>A
|
ENSP00000340557.5:p.Gly688Asp
|
|
ENST00000484589.2:c.615G>A
|
|
|
ENST00000642213.1:n.545G>A
|
|
|
ENST00000642660.1:n.943G>A
|
|
|
ENST00000643859.1:c.954G>A
|
|
|
ENST00000643915.1:c.377G>A
|
ENSP00000496187.1:p.Gly126Asp
|
|
ENST00000646039.1:c.1403G>A
|
ENSP00000494168.1:p.Gly468Asp
|
|
ENST00000646437.1:c.697G>A
|
|
|
ENST00000647453.1:n.1132G>A
|
|
|
ENST00000647518.1:n.3900G>A
|
|
|
ENST00000181839.8:c.2063G>A
|
ENSP00000181839.4:p.Gly688Asp
|
|
ENST00000340829.9:c.2063G>A
|
ENSP00000340557.5:p.Gly688Asp
|
|
ENST00000484589.1:n.615G>A
|
|
|
ENST00000611390.1:c.221G>A
|
ENSP00000484610.1:p.Gly74Asp
|
|
ENST00000613626.4:c.221G>A
|
ENSP00000480835.1:p.Gly74Asp
|
|
NM_003718.4:c.2063G>A
|
NP_003709.3:p.Gly688Asp
|
|
NM_031267.3:c.2063G>A
|
NP_112557.2:p.Gly688Asp
|
|
XM_011515597.1:c.2063G>A
|
XP_011513899.1:p.Gly688Asp
|
|
XM_011515598.1:c.2063G>A
|
XP_011513900.1:p.Gly688Asp
|
|
XM_011515597.3:c.2063G>A
|
XP_011513899.1:p.Gly688Asp
|
|
XM_017012750.2:c.2063G>A
|
XP_016868239.1:p.Gly688Asp
|
|
XM_017012751.2:c.2063G>A
|
XP_016868240.1:p.Gly688Asp
|
|
NM_003718.5:c.2063G>A
MANE Select
|
NP_003709.3:p.Gly688Asp
|
|