ENST00000376059.8:c.178A>C
MANE Select
|
ENSP00000365227.3:p.Asn60His
|
|
ENST00000337917.11:c.220A>C
|
ENSP00000338776.7:p.Asn74His
|
|
ENST00000376049.4:c.16A>C
|
ENSP00000365217.4:p.Asn6His
|
|
ENST00000376059.7:c.178A>C
|
ENSP00000365227.3:p.Asn60His
|
|
ENST00000466820.1:n.595A>C
|
|
|
ENST00000497362.5:n.597A>C
|
|
|
NM_001623.3:c.178A>C
|
NP_001614.3:p.Asn60His
|
|
NM_004847.3:c.16A>C
|
NP_004838.1:p.Asn6His
|
|
NM_032955.1:c.16A>C
|
NP_116573.1:p.Asn6His
|
|
XM_005248870.3:c.178A>C
|
XP_005248927.1:p.Asn60His
|
|
XM_005248871.1:c.241A>C
|
XP_005248928.1:p.Asn81His
|
|
NM_001318970.1:c.16A>C
|
NP_001305899.1:p.Asn6His
|
|
NM_001623.4:c.178A>C
|
NP_001614.3:p.Asn60His
|
|
NM_032955.2:c.16A>C
|
NP_116573.1:p.Asn6His
|
|
XM_005248870.4:c.178A>C
|
XP_005248927.1:p.Asn60His
|
|
XM_017010332.1:c.16A>C
|
XP_016865821.1:p.Asn6His
|
|
NM_001623.5:c.178A>C
MANE Select
|
NP_001614.3:p.Asn60His
|
|
NM_001318970.2:c.16A>C
|
NP_001305899.1:p.Asn6His
|
|
NM_032955.3:c.16A>C
|
NP_116573.1:p.Asn6His
|
|