ENST00000270357.10:c.1511-451T>G
MANE Select
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ENSP00000270357.4:n.1511-451T>G
|
|
ENST00000270357.8:c.818-451T>G
|
ENSP00000270357.3:n.818-451T>G
|
|
ENST00000437406.1:c.109+474T>G
|
ENSP00000403319.1:n.109+474T>G
|
|
ENST00000451363.5:c.152-451T>G
|
ENSP00000414661.1:n.152-451T>G
|
|
ENST00000464550.5:n.347-451T>G
|
|
|
ENST00000471657.1:n.314-451T>G
|
|
|
ENST00000481757.5:n.1994T>G
|
|
|
ENST00000486058.5:n.1624-451T>G
|
|
|
ENST00000493398.5:n.657-451T>G
|
|
|
NM_018226.4:c.1511-451T>G
|
NP_060696.4:n.1511-451T>G
|
|
XM_005247036.3:c.1510+474T>G
|
XP_005247093.1:n.1510+474T>G
|
|
NM_018226.5:c.1511-451T>G
|
NP_060696.4:n.1511-451T>G
|
|
XM_005247036.4:c.1510+474T>G
|
XP_005247093.1:n.1510+474T>G
|
|
NM_018226.6:c.1511-451T>G
MANE Select
|
NP_060696.4:n.1511-451T>G
|
|