ENST00000244360.8:c.478+182G=
MANE Select
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ENSP00000244360.7:n.478+182G=
|
|
ENST00000244360.7:c.478+182G=
|
ENSP00000244360.7:n.478+182G=
|
|
ENST00000376751.8:c.478+182G=
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ENSP00000365942.4:n.478+182G=
|
|
ENST00000244360.6:c.682+182G=
|
ENSP00000244360.6:n.682+182G=
|
|
ENST00000376751.7:c.682+182G=
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ENSP00000365942.3:n.682+182G=
|
|
NM_025236.3:c.682+182G=
|
NP_079512.2:n.682+182G=
|
|
NM_170769.2:c.682+182G=
|
NP_739575.2:n.682+182G=
|
|
XM_017011325.1:c.223+182G=
|
XP_016866814.1:n.223+182G=
|
|
XM_017011326.1:c.682+182G=
|
XP_016866815.1:n.682+182G=
|
|
NM_025236.4:c.478+182G=
MANE Select
|
NP_079512.3:n.478+182G=
|
|
NM_170769.3:c.478+182G=
|
NP_739575.3:n.478+182G=
|
|