ENST00000534624.6:c.1569G>C
MANE Select
|
ENSP00000432083.1:p.Glu523Asp
|
|
ENST00000227378.7:c.1569G>C
|
ENSP00000227378.3:p.Glu523Asp
|
|
ENST00000453788.6:c.1387+329G>C
|
ENSP00000404372.2:n.1387+329G>C
|
|
ENST00000524552.5:c.342G>C
|
ENSP00000435908.1:p.Glu114Asp
|
|
ENST00000526110.5:c.1512G>C
|
ENSP00000433584.1:p.Glu504Asp
|
|
ENST00000526686.1:c.225G>C
|
ENSP00000435019.1:p.Glu75Asp
|
|
ENST00000532091.1:n.1691G>C
|
|
|
ENST00000532636.5:c.1569G>C
|
ENSP00000437125.1:p.Glu523Asp
|
|
ENST00000533540.5:c.1131G>C
|
ENSP00000437189.1:p.Glu377Asp
|
|
ENST00000534319.5:c.861G>C
|
ENSP00000433316.1:p.Glu287Asp
|
|
ENST00000534624.5:c.1569G>C
|
ENSP00000432083.1:p.Glu523Asp
|
|
NM_006597.5:c.1569G>C
|
NP_006588.1:p.Glu523Asp
|
|
NM_153201.3:c.1387+329G>C
|
NP_694881.1:n.1387+329G>C
|
|
XM_011542798.1:c.1569G>C
|
XP_011541100.1:p.Glu523Asp
|
|
NM_006597.6:c.1569G>C
MANE Select
|
NP_006588.1:p.Glu523Asp
|
|
NM_153201.4:c.1387+329G>C
|
NP_694881.1:n.1387+329G>C
|
|