ENST00000251810.8:c.975G>C
MANE Select
|
ENSP00000251810.3:p.Glu325Asp
|
|
ENST00000251810.7:c.975G>C
|
ENSP00000251810.3:p.Glu325Asp
|
|
ENST00000395910.6:n.362G>C
|
|
|
ENST00000395912.6:c.819G>C
|
ENSP00000379248.2:p.Glu273Asp
|
|
ENST00000519317.5:c.339G>C
|
ENSP00000430641.1:p.Glu113Asp
|
|
ENST00000519962.5:c.120G>C
|
ENSP00000429140.1:p.Glu40Asp
|
|
ENST00000522368.5:c.1144G>C
|
|
|
ENST00000522394.1:c.308G>C
|
ENSP00000429578.1:n.308G>C
|
|
ENST00000621845.1:c.813G>C
|
ENSP00000484318.1:p.Glu271Asp
|
|
NM_001172477.1:c.1191G>C , LRG_788t1:c.1191G>C
|
NP_001165948.1:p.Glu397Asp
|
|
NM_001172478.1:c.819G>C
|
NP_001165949.1:p.Glu273Asp
|
|
NM_015713.4:c.975G>C , LRG_788t2:c.975G>C
|
NP_056528.2:p.Glu325Asp
|
|
NM_001172478.2:c.819G>C
|
NP_001165949.1:p.Glu273Asp
|
|
NM_015713.5:c.975G>C
MANE Select
|
NP_056528.2:p.Glu325Asp
|
|