ENST00000465218.3:n.1183A>G
|
|
|
ENST00000468748.7:n.1403A>G
|
|
|
ENST00000484154.2:n.1390A>G
|
|
|
ENST00000491008.6:n.1908A>G
|
|
|
ENST00000492226.2:n.1427A>G
|
|
|
ENST00000492773.6:c.914A>G
|
|
|
ENST00000647636.1:c.*9A>G
|
ENSP00000497505.1:n.*9A>G
|
|
ENST00000647909.1:c.1184A>G
|
ENSP00000498164.1:p.Asp395Gly
|
|
ENST00000648145.1:c.932A>G
|
|
|
ENST00000648189.1:c.978A>G
|
|
|
ENST00000648256.1:c.1132A>G
|
ENSP00000497356.1:n.1132A>G
|
|
ENST00000648314.1:c.*279A>G
|
ENSP00000496920.1:n.*279A>G
|
|
ENST00000648599.1:c.*443A>G
|
ENSP00000497159.1:n.*443A>G
|
|
ENST00000648630.1:c.1039A>G
|
ENSP00000497887.1:p.Ile347Val
|
|
ENST00000648682.1:c.1170A>G
|
ENSP00000498185.1:p.Ter390Trp
|
|
ENST00000648882.1:c.*986A>G
|
ENSP00000497603.1:n.*986A>G
|
|
ENST00000648890.1:c.1160A>G
|
ENSP00000497503.1:p.Asp387Gly
|
|
ENST00000648915.2:c.1160A>G
MANE Select
|
ENSP00000497160.1:p.Asp387Gly
|
|
ENST00000649545.1:c.581A>G
|
|
|
ENST00000649688.1:c.*453A>G
|
ENSP00000497097.1:n.*453A>G
|
|
ENST00000649814.1:n.1209A>G
|
|
|
ENST00000650270.1:c.1027A>G
|
|
|
ENST00000273783.7:c.1160A>G
|
ENSP00000273783.3:p.Asp387Gly
|
|
ENST00000432982.5:c.246-309A>G
|
|
|
ENST00000444495.1:c.1160A>G
|
ENSP00000409142.1:p.Asp387Gly
|
|
ENST00000479833.1:n.361A>G
|
|
|
ENST00000481054.5:n.1254A>G
|
|
|
ENST00000491144.5:n.1664A>G
|
|
|
ENST00000492773.5:n.43A>G
|
|
|
NM_003907.2:c.1160A>G
|
NP_003898.2:p.Asp387Gly
|
|
XM_011513265.1:c.410A>G
|
XP_011511567.1:p.Asp137Gly
|
|
XM_011513266.1:c.323A>G
|
XP_011511568.1:p.Asp108Gly
|
|
XR_924208.1:n.2111A>G
|
|
|
NM_003907.3:c.1160A>G
MANE Select
|
NP_003898.2:p.Asp387Gly
|
|
XM_011513266.3:c.323A>G
|
XP_011511568.1:p.Asp108Gly
|
|
XR_001740352.2:n.1523A>G
|
|
|
XR_001740353.2:n.1523A>G
|
|
|
XR_924208.2:n.1523A>G
|
|
|