|
ENST00000486121.7:c.*520G>C
(GLA)
|
ENSP00000501124.2:n.*520G>C
|
|
|
ENST00000674127.2:c.*577G>C
(GLA)
|
ENSP00000501044.2:n.*577G>C
|
|
|
ENST00000710365.1:c.1149G>C
(GLA)
|
ENSP00000518234.1:p.Glu383Asp
|
|
|
ENST00000218516.4:c.1074G>C
(GLA)
MANE Select
|
ENSP00000218516.4:p.Glu358Asp
|
|
|
ENST00000466414.2:n.1210G>C
(GLA)
|
|
|
|
ENST00000468823.2:n.2496G>C
(GLA)
|
|
|
|
ENST00000479445.2:n.1688G>C
(GLA)
|
|
|
|
ENST00000480513.6:c.*382G>C
(GLA)
|
ENSP00000497055.1:n.*382G>C
|
|
|
ENST00000486121.6:c.1119G>C
(GLA)
|
|
|
|
ENST00000649178.1:c.1197G>C
(GLA)
|
ENSP00000498186.1:p.Glu399Asp
|
|
|
ENST00000674127.1:c.1174G>C
(GLA)
|
ENSP00000501044.1:n.1174G>C
|
|
|
ENST00000674142.1:n.1378G>C
(GLA)
|
|
|
|
ENST00000675592.1:c.876G>C
(GLA)
|
ENSP00000502239.1:p.Glu292Asp
|
|
|
ENST00000675799.1:c.*599G>C
(GLA)
|
ENSP00000502661.1:n.*599G>C
|
|
|
ENST00000675968.1:n.3945G>C
(GLA)
|
|
|
|
ENST00000676156.1:c.1038G>C
(GLA)
|
ENSP00000501730.1:p.Glu346Asp
|
|
|
ENST00000676372.1:c.1140G>C
(GLA)
|
ENSP00000502805.1:n.1140G>C
|
|
|
ENST00000218516.3:c.1074G>C
(GLA)
|
ENSP00000218516.3:p.Glu358Asp
|
|
|
ENST00000409170.3:c.300+2568C>G
(RPL36A-HNRNPH2)
|
ENSP00000386655.4:n.300+2568C>G
|
|
|
ENST00000409338.5:c.177+6203C>G
(RPL36A-HNRNPH2)
|
ENSP00000386974.2:n.177+6203C>G
|
|
|
ENST00000466414.1:n.400G>C
(GLA)
|
|
|
|
ENST00000493905.6:c.*462G>C
(GLA)
|
ENSP00000476935.1:n.*462G>C
|
|
|
NM_000169.2:c.1074G>C , LRG_672t1:c.1074G>C
(GLA)
|
NP_000160.1:p.Glu358Asp
|
|
|
NM_001199973.1:c.408+2568C>G
(RPL36A-HNRNPH2)
|
NP_001186902.1:n.408+2568C>G
|
|
|
NM_001199974.1:c.285+6203C>G
(RPL36A-HNRNPH2)
|
NP_001186903.1:n.285+6203C>G
|
|
|
XR_938397.1:n.1159G>C
(GLA)
|
|
|
|
XR_938397.2:n.1180G>C
(GLA)
|
|
|
|
NM_001199973.2:c.300+2568C>G
(RPL36A-HNRNPH2)
|
NP_001186902.2:n.300+2568C>G
|
|
|
NM_001199974.2:c.177+6203C>G
(RPL36A-HNRNPH2)
|
NP_001186903.2:n.177+6203C>G
|
|
|
NM_000169.3:c.1074G>C
(GLA)
MANE Select
|
NP_000160.1:p.Glu358Asp
|
|
|
NR_164783.1:n.1153G>C
(GLA)
|
|
|
