ENST00000348974.5:c.1596A>G
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ENSP00000330021.7:p.Thr532=
|
|
ENST00000394236.9:c.1596A>G
MANE Select
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ENSP00000377783.3:p.Thr532=
|
|
ENST00000407433.6:c.1551A>G
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ENSP00000385794.2:p.Thr517=
|
|
ENST00000647936.1:c.1596A>G
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ENSP00000496822.1:p.Thr532=
|
|
ENST00000648381.1:n.1764A>G
|
|
|
ENST00000648853.1:c.1554A>G
|
ENSP00000497262.1:p.Thr518=
|
|
ENST00000649103.1:c.1695A>G
|
ENSP00000497962.1:n.1695A>G
|
|
ENST00000649585.1:c.539A>G
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ENSP00000498163.1:n.539A>G
|
|
ENST00000650591.1:c.1692A>G
|
ENSP00000497376.1:p.Thr564=
|
|
ENST00000394236.7:c.1596A>G
|
ENSP00000377783.3:p.Thr532=
|
|
ENST00000407433.5:c.1203A>G
|
ENSP00000385794.1:p.Thr401=
|
|
NM_000313.3:c.1596A>G , LRG_572t1:c.1596A>G
|
NP_000304.2:p.Thr532=
|
|
NM_001314077.1:c.1692A>G , LRG_572t2:c.1692A>G
|
NP_001301006.1:p.Thr564=
|
|
NM_000313.4:c.1596A>G
MANE Select
|
NP_000304.2:p.Thr532=
|
|
NM_001314077.2:c.1692A>G
|
NP_001301006.1:p.Thr564=
|
|