ENST00000427262.6:c.528T=
|
ENSP00000405052.1:p.Asn176=
|
|
ENST00000642232.1:c.708T=
|
ENSP00000494064.1:p.Asn236=
|
|
ENST00000643230.2:c.708T=
MANE Select
|
ENSP00000496491.1:p.Asn236=
|
|
ENST00000643441.1:n.693T=
|
|
|
ENST00000644381.1:n.271T=
|
|
|
ENST00000307792.7:c.708T=
|
ENSP00000303212.3:p.Asn236=
|
|
ENST00000427262.5:c.528T=
|
ENSP00000405052.1:p.Asn176=
|
|
NM_001178129.1:c.528T=
|
NP_001171600.1:p.Asn176=
|
|
NM_012431.2:c.708T=
|
NP_036563.1:p.Asn236=
|
|
XM_011516715.1:c.708T=
|
XP_011515017.1:p.Asn236=
|
|
NM_012431.3:c.708T=
MANE Select
|
NP_036563.1:p.Asn236=
|
|
NM_001178129.2:c.528T=
|
NP_001171600.1:p.Asn176=
|
|