ENST00000360215.3:c.514C>A
MANE Select
|
ENSP00000353346.1:p.His172Asn
|
|
ENST00000496656.2:n.293C>A
|
|
|
ENST00000651132.1:c.514C>A
|
ENSP00000498322.1:p.His172Asn
|
|
ENST00000651676.1:c.514C>A
|
ENSP00000498699.1:p.His172Asn
|
|
ENST00000651994.1:c.*70-4790C>A
|
ENSP00000498310.1:n.*70-4790C>A
|
|
ENST00000652718.1:c.346C>A
|
ENSP00000498866.1:p.His116Asn
|
|
ENST00000360215.2:c.514C>A
|
ENSP00000353346.1:p.His172Asn
|
|
ENST00000496656.1:n.293C>A
|
|
|
NM_182548.3:c.514C>A
|
NP_872354.1:p.His172Asn
|
|
XM_011514403.1:c.514C>A
|
XP_011512705.1:p.His172Asn
|
|
NM_182548.4:c.514C>A
MANE Select
|
NP_872354.1:p.His172Asn
|
|