|
ENST00000674127.2:c.*728C>T
(GLA)
|
ENSP00000501044.2:n.*728C>T
|
|
|
ENST00000710365.1:c.1300C>T
(GLA)
|
ENSP00000518234.1:p.Pro434Ser
|
|
|
ENST00000218516.4:c.1225C>T
(GLA)
MANE Select
|
ENSP00000218516.4:p.Pro409Ser
|
|
|
ENST00000466414.2:n.1361C>T
(GLA)
|
|
|
|
ENST00000468823.2:n.2647C>T
(GLA)
|
|
|
|
ENST00000479445.2:n.1839C>T
(GLA)
|
|
|
|
ENST00000649178.1:c.1348C>T
(GLA)
|
ENSP00000498186.1:p.Pro450Ser
|
|
|
ENST00000674127.1:c.1325C>T
(GLA)
|
ENSP00000501044.1:n.1325C>T
|
|
|
ENST00000674142.1:n.1421+108C>T
(GLA)
|
|
|
|
ENST00000675592.1:c.1027C>T
(GLA)
|
ENSP00000502239.1:p.Pro343Ser
|
|
|
ENST00000675799.1:c.*750C>T
(GLA)
|
ENSP00000502661.1:n.*750C>T
|
|
|
ENST00000675968.1:n.4096C>T
(GLA)
|
|
|
|
ENST00000676156.1:c.1189C>T
(GLA)
|
ENSP00000501730.1:p.Pro397Ser
|
|
|
ENST00000676372.1:c.1291C>T
(GLA)
|
ENSP00000502805.1:n.1291C>T
|
|
|
ENST00000218516.3:c.1225C>T
(GLA)
|
ENSP00000218516.3:p.Pro409Ser
|
|
|
ENST00000409170.3:c.300+2417G>A
(RPL36A-HNRNPH2)
|
ENSP00000386655.4:n.300+2417G>A
|
|
|
ENST00000409338.5:c.177+6052G>A
(RPL36A-HNRNPH2)
|
ENSP00000386974.2:n.177+6052G>A
|
|
|
ENST00000466414.1:n.551C>T
(GLA)
|
|
|
|
ENST00000493905.6:c.*613C>T
(GLA)
|
ENSP00000476935.1:n.*613C>T
|
|
|
NM_000169.2:c.1225C>T , LRG_672t1:c.1225C>T
(GLA)
|
NP_000160.1:p.Pro409Ser
|
|
|
NM_001199973.1:c.408+2417G>A
(RPL36A-HNRNPH2)
|
NP_001186902.1:n.408+2417G>A
|
|
|
NM_001199974.1:c.285+6052G>A
(RPL36A-HNRNPH2)
|
NP_001186903.1:n.285+6052G>A
|
|
|
XR_938397.1:n.1310C>T
(GLA)
|
|
|
|
XR_938397.2:n.1331C>T
(GLA)
|
|
|
|
NM_001199973.2:c.300+2417G>A
(RPL36A-HNRNPH2)
|
NP_001186902.2:n.300+2417G>A
|
|
|
NM_001199974.2:c.177+6052G>A
(RPL36A-HNRNPH2)
|
NP_001186903.2:n.177+6052G>A
|
|
|
NM_000169.3:c.1225C>T
(GLA)
MANE Select
|
NP_000160.1:p.Pro409Ser
|
|
|
NR_164783.1:n.1304C>T
(GLA)
|
|
|
