ENST00000426263.10:c.407C>A
MANE Select
|
ENSP00000416293.2:p.Thr136Asn
|
|
ENST00000674765.1:c.407C>A
|
ENSP00000501811.1:p.Thr136Asn
|
|
ENST00000675112.1:n.430C>A
|
|
|
ENST00000676254.1:n.856C>A
|
|
|
ENST00000372500.4:c.311C>A
|
ENSP00000361578.4:p.Thr104Asn
|
|
ENST00000426263.7:c.407C>A
|
ENSP00000416293.2:p.Thr136Asn
|
|
ENST00000439722.2:c.286C>A
|
ENSP00000395521.2:n.286C>A
|
|
ENST00000475162.3:c.306C>A
|
|
|
ENST00000625233.2:n.615C>A
|
|
|
ENST00000630287.2:c.407C>A
|
ENSP00000486694.1:p.Thr136Asn
|
|
NM_006516.2:c.407C>A
|
NP_006507.2:p.Thr136Asn
|
|
NM_006516.3:c.407C>A
|
NP_006507.2:p.Thr136Asn
|
|
NM_006516.4:c.407C>A
MANE Select
|
NP_006507.2:p.Thr136Asn
|
|