ENST00000698724.1:n.1936T>G
|
|
|
ENST00000698725.1:n.1689T>G
|
|
|
ENST00000698726.1:n.3249T>G
|
|
|
ENST00000698727.1:n.2982T>G
|
|
|
ENST00000698728.1:n.3598T>G
|
|
|
ENST00000698729.1:n.5046T>G
|
|
|
ENST00000698730.1:n.5144T>G
|
|
|
ENST00000698731.1:c.3878T>G
|
ENSP00000513898.1:p.Val1293Gly
|
|
ENST00000698732.1:c.*2708T>G
|
ENSP00000513899.1:n.*2708T>G
|
|
ENST00000698733.1:c.*3206T>G
|
ENSP00000513900.1:n.*3206T>G
|
|
ENST00000698734.1:c.*2192T>G
|
ENSP00000513901.1:n.*2192T>G
|
|
ENST00000698735.1:n.4370T>G
|
|
|
ENST00000698736.1:n.4783T>G
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|
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ENST00000698737.1:n.4134T>G
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|
|
ENST00000372371.8:c.4019T>G
MANE Select
|
ENSP00000361446.3:p.Val1340Gly
|
|
ENST00000372371.7:c.4019T>G
|
ENSP00000361446.3:p.Val1340Gly
|
|
ENST00000616246.4:c.467T>G
|
ENSP00000483738.1:p.Val156Gly
|
|
NM_007055.3:c.4019T>G
|
NP_008986.2:p.Val1340Gly
|
|
NM_007055.4:c.4019T>G
MANE Select
|
NP_008986.2:p.Val1340Gly
|
|