|
ENST00000486121.7:c.*567A>C
(GLA)
|
ENSP00000501124.2:n.*567A>C
|
|
|
ENST00000674127.2:c.*624A>C
(GLA)
|
ENSP00000501044.2:n.*624A>C
|
|
|
ENST00000710365.1:c.1196A>C
(GLA)
|
ENSP00000518234.1:p.Lys399Thr
|
|
|
ENST00000218516.4:c.1121A>C
(GLA)
MANE Select
|
ENSP00000218516.4:p.Lys374Thr
|
|
|
ENST00000466414.2:n.1257A>C
(GLA)
|
|
|
|
ENST00000468823.2:n.2543A>C
(GLA)
|
|
|
|
ENST00000479445.2:n.1735A>C
(GLA)
|
|
|
|
ENST00000480513.6:c.*429A>C
(GLA)
|
ENSP00000497055.1:n.*429A>C
|
|
|
ENST00000486121.6:c.1166A>C
(GLA)
|
|
|
|
ENST00000649178.1:c.1244A>C
(GLA)
|
ENSP00000498186.1:p.Lys415Thr
|
|
|
ENST00000674127.1:c.1221A>C
(GLA)
|
ENSP00000501044.1:n.1221A>C
|
|
|
ENST00000674142.1:n.1421+4A>C
(GLA)
|
|
|
|
ENST00000675592.1:c.923A>C
(GLA)
|
ENSP00000502239.1:p.Lys308Thr
|
|
|
ENST00000675799.1:c.*646A>C
(GLA)
|
ENSP00000502661.1:n.*646A>C
|
|
|
ENST00000675968.1:n.3992A>C
(GLA)
|
|
|
|
ENST00000676156.1:c.1085A>C
(GLA)
|
ENSP00000501730.1:p.Lys362Thr
|
|
|
ENST00000676372.1:c.1187A>C
(GLA)
|
ENSP00000502805.1:n.1187A>C
|
|
|
ENST00000218516.3:c.1121A>C
(GLA)
|
ENSP00000218516.3:p.Lys374Thr
|
|
|
ENST00000409170.3:c.300+2521T>G
(RPL36A-HNRNPH2)
|
ENSP00000386655.4:n.300+2521T>G
|
|
|
ENST00000409338.5:c.177+6156T>G
(RPL36A-HNRNPH2)
|
ENSP00000386974.2:n.177+6156T>G
|
|
|
ENST00000466414.1:n.447A>C
(GLA)
|
|
|
|
ENST00000493905.6:c.*509A>C
(GLA)
|
ENSP00000476935.1:n.*509A>C
|
|
|
NM_000169.2:c.1121A>C , LRG_672t1:c.1121A>C
(GLA)
|
NP_000160.1:p.Lys374Thr
|
|
|
NM_001199973.1:c.408+2521T>G
(RPL36A-HNRNPH2)
|
NP_001186902.1:n.408+2521T>G
|
|
|
NM_001199974.1:c.285+6156T>G
(RPL36A-HNRNPH2)
|
NP_001186903.1:n.285+6156T>G
|
|
|
XR_938397.1:n.1206A>C
(GLA)
|
|
|
|
XR_938397.2:n.1227A>C
(GLA)
|
|
|
|
NM_001199973.2:c.300+2521T>G
(RPL36A-HNRNPH2)
|
NP_001186902.2:n.300+2521T>G
|
|
|
NM_001199974.2:c.177+6156T>G
(RPL36A-HNRNPH2)
|
NP_001186903.2:n.177+6156T>G
|
|
|
NM_000169.3:c.1121A>C
(GLA)
MANE Select
|
NP_000160.1:p.Lys374Thr
|
|
|
NR_164783.1:n.1200A>C
(GLA)
|
|
|
