ENST00000367435.5:c.1002T>C
MANE Select
|
ENSP00000356405.4:p.Thr334=
|
|
ENST00000635846.1:c.759T>C
|
ENSP00000490035.1:p.Thr253=
|
|
ENST00000643006.1:c.1070T>C
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ENSP00000496633.1:p.Leu357Pro
|
|
ENST00000648071.1:c.*978T>C
|
ENSP00000497513.1:n.*978T>C
|
|
ENST00000649613.1:n.252T>C
|
|
|
ENST00000649895.1:n.1220T>C
|
|
|
ENST00000650197.1:c.1002T>C
|
ENSP00000496929.1:p.Thr334=
|
|
ENST00000367435.3:c.1002T>C
|
ENSP00000356405.3:p.Thr334=
|
|
NM_024529.4:c.1002T>C , LRG_507t1:c.1002T>C
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NP_078805.3:p.Thr334=
|
|
NM_024529.5:c.1002T>C
MANE Select
|
NP_078805.3:p.Thr334=
|
|