ENST00000703783.1:n.615T>A
|
|
|
ENST00000703785.1:n.696T>A
|
|
|
ENST00000262464.9:c.3831T>A
MANE Select
|
ENSP00000262464.4:p.Asp1277Glu
|
|
ENST00000262464.8:c.3831T>A
|
ENSP00000262464.4:p.Asp1277Glu
|
|
ENST00000507835.5:c.381T>A
|
ENSP00000426839.1:p.Asp127Glu
|
|
ENST00000508053.5:c.3831T>A
|
ENSP00000424571.1:p.Asp1277Glu
|
|
ENST00000508989.5:c.3732T>A
|
ENSP00000425596.1:p.Asp1244Glu
|
|
ENST00000619499.4:c.3828T>A
|
ENSP00000482132.1:p.Asp1276Glu
|
|
NM_001999.3:c.3831T>A
|
NP_001990.2:p.Asp1277Glu
|
|
XM_017009228.2:c.3678T>A
|
XP_016864717.1:p.Asp1226Glu
|
|
NM_001999.4:c.3831T>A
MANE Select
|
NP_001990.2:p.Asp1277Glu
|
|