ENST00000439176.6:c.423G>C
|
ENSP00000408344.2:p.Glu141Asp
|
|
ENST00000647431.2:c.524G>C
|
ENSP00000494726.2:n.524G>C
|
|
ENST00000647486.2:c.423G>C
|
ENSP00000494466.2:p.Glu141Asp
|
|
ENST00000675042.2:c.249G>C
|
ENSP00000502082.2:p.Glu83Asp
|
|
ENST00000675452.2:c.*388G>C
|
ENSP00000506954.1:n.*388G>C
|
|
ENST00000682217.1:c.423G>C
|
ENSP00000507570.1:p.Glu141Asp
|
|
ENST00000682246.1:n.479G>C
|
|
|
ENST00000682375.1:c.*253G>C
|
ENSP00000507551.1:n.*253G>C
|
|
ENST00000683052.1:c.225G>C
|
ENSP00000507072.1:p.Glu75Asp
|
|
ENST00000683199.1:n.445G>C
|
|
|
ENST00000683216.1:n.688G>C
|
|
|
ENST00000683460.1:c.*253G>C
|
ENSP00000507820.1:n.*253G>C
|
|
ENST00000684394.1:n.478G>C
|
|
|
ENST00000684453.1:n.473G>C
|
|
|
ENST00000684621.1:n.479G>C
|
|
|
ENST00000265038.10:c.423G>C
|
ENSP00000265038.6:p.Glu141Asp
|
|
ENST00000497892.6:c.*221G>C
|
ENSP00000501805.1:n.*221G>C
|
|
ENST00000643034.1:c.*315G>C
|
ENSP00000496080.1:n.*315G>C
|
|
ENST00000643708.1:c.*253G>C
|
ENSP00000494199.1:n.*253G>C
|
|
ENST00000647431.1:c.475G>C
|
|
|
ENST00000647486.1:c.374G>C
|
|
|
ENST00000675042.1:c.249G>C
|
ENSP00000502082.1:p.Glu83Asp
|
|
ENST00000675229.1:c.423G>C
|
ENSP00000502154.1:p.Glu141Asp
|
|
ENST00000675378.1:c.423G>C
|
ENSP00000502535.1:p.Glu141Asp
|
|
ENST00000675452.1:n.672G>C
|
|
|
ENST00000675920.1:n.1031G>C
|
|
|
ENST00000676185.1:c.423G>C
MANE Select
|
ENSP00000501614.1:p.Glu141Asp
|
|
ENST00000265038.9:c.423G>C
|
ENSP00000265038.5:p.Glu141Asp
|
|
ENST00000381118.7:c.*467G>C
|
ENSP00000370510.3:n.*467G>C
|
|
ENST00000439176.5:c.249G>C
|
ENSP00000408344.1:p.Glu83Asp
|
|
ENST00000462279.5:n.268G>C
|
|
|
ENST00000484330.5:n.227-2342G>C
|
|
|
ENST00000495985.5:n.196G>C
|
|
|
ENST00000497892.5:n.466G>C
|
|
|
NM_000082.3:c.423G>C , LRG_466t1:c.423G>C
|
NP_000073.1:p.Glu141Asp
|
|
NM_001007233.2:c.249G>C
|
NP_001007234.1:p.Glu83Asp
|
|
NM_001007234.2:c.423G>C
|
NP_001007235.1:p.Glu141Asp
|
|
NM_001290285.1:c.23-1134G>C
|
NP_001277214.1:n.23-1134G>C
|
|
NM_001007234.3:c.423G>C
|
NP_001007235.1:p.Glu141Asp
|
|
NM_000082.4:c.423G>C
MANE Select
|
NP_000073.1:p.Glu141Asp
|
|
NM_001007233.3:c.249G>C
|
NP_001007234.1:p.Glu83Asp
|
|
NM_001290285.2:c.23-1134G>C
|
NP_001277214.1:n.23-1134G>C
|
|