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NM_000169.3:c.1165C>G
(GLA)
MANE Select
|
NP_000160.1:p.Pro389Ala
|
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ENST00000218516.4:c.1165C>G
(GLA)
MANE Select
|
ENSP00000218516.4:p.Pro389Ala
|
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NM_000169.2:c.1165C>G , LRG_672t1:c.1165C>G
(GLA)
|
NP_000160.1:p.Pro389Ala
|
|
NM_001199973.1:c.408+2477G>C
(RPL36A-HNRNPH2)
|
NP_001186902.1:n.408+2477G>C
|
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NM_001199973.2:c.300+2477G>C
(RPL36A-HNRNPH2)
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NP_001186902.2:n.300+2477G>C
|
|
NM_001199974.1:c.285+6112G>C
(RPL36A-HNRNPH2)
|
NP_001186903.1:n.285+6112G>C
|
|
NM_001199974.2:c.177+6112G>C
(RPL36A-HNRNPH2)
|
NP_001186903.2:n.177+6112G>C
|
|
NR_164783.1:n.1244C>G
(GLA)
|
|
|
ENST00000218516.3:c.1165C>G
(GLA)
|
ENSP00000218516.3:p.Pro389Ala
|
|
ENST00000409170.3:c.300+2477G>C
(RPL36A-HNRNPH2)
|
ENSP00000386655.4:n.300+2477G>C
|
|
ENST00000409338.5:c.177+6112G>C
(RPL36A-HNRNPH2)
|
ENSP00000386974.2:n.177+6112G>C
|
|
ENST00000466414.1:n.491C>G
(GLA)
|
|
|
ENST00000466414.2:n.1301C>G
(GLA)
|
|
|
ENST00000468823.2:n.2587C>G
(GLA)
|
|
|
ENST00000479445.2:n.1779C>G
(GLA)
|
|
|
ENST00000493905.6:c.*553C>G
(GLA)
|
ENSP00000476935.1:n.*553C>G
|
|
ENST00000649178.1:c.1288C>G
(GLA)
|
ENSP00000498186.1:p.Pro430Ala
|
|
ENST00000674127.1:c.1265C>G
(GLA)
|
ENSP00000501044.1:n.1265C>G
|
|
ENST00000674127.2:c.*668C>G
(GLA)
|
ENSP00000501044.2:n.*668C>G
|
|
ENST00000674142.1:n.1421+48C>G
(GLA)
|
|
|
ENST00000675592.1:c.967C>G
(GLA)
|
ENSP00000502239.1:p.Pro323Ala
|
|
ENST00000675799.1:c.*690C>G
(GLA)
|
ENSP00000502661.1:n.*690C>G
|
|
ENST00000675968.1:n.4036C>G
(GLA)
|
|
|
ENST00000676156.1:c.1129C>G
(GLA)
|
ENSP00000501730.1:p.Pro377Ala
|
|
ENST00000676372.1:c.1231C>G
(GLA)
|
ENSP00000502805.1:n.1231C>G
|
|
ENST00000710365.1:c.1240C>G
(GLA)
|
ENSP00000518234.1:p.Pro414Ala
|
|
XR_938397.1:n.1250C>G
(GLA)
|
|
|
XR_938397.2:n.1271C>G
(GLA)
|
|