ENST00000426263.10:c.496G=
MANE Select
|
ENSP00000416293.2:p.Val166=
|
|
ENST00000674765.1:c.496G=
|
ENSP00000501811.1:p.Val166=
|
|
ENST00000675112.1:n.519G=
|
|
|
ENST00000676254.1:n.945G=
|
|
|
ENST00000426263.7:c.496G=
|
ENSP00000416293.2:p.Val166=
|
|
ENST00000439722.2:c.375G=
|
ENSP00000395521.2:n.375G=
|
|
ENST00000475162.3:c.395G=
|
|
|
ENST00000625233.2:n.704G=
|
|
|
ENST00000630287.2:c.496G=
|
ENSP00000486694.1:p.Val166=
|
|
NM_006516.2:c.496G=
|
NP_006507.2:p.Val166=
|
|
NM_006516.3:c.496G=
|
NP_006507.2:p.Val166=
|
|
NM_006516.4:c.496G=
MANE Select
|
NP_006507.2:p.Val166=
|
|