ENST00000456935.7:c.398A>C
MANE Select
|
ENSP00000395473.2:p.Asn133Thr
|
|
ENST00000221363.8:c.398A>C
|
ENSP00000221363.4:p.Asn133Thr
|
|
ENST00000456935.6:c.398A>C
|
ENSP00000395473.2:p.Asn133Thr
|
|
ENST00000466794.5:n.380A>C
|
|
|
ENST00000486847.2:c.295A>C
|
ENSP00000470174.1:p.Met99Leu
|
|
ENST00000596512.5:n.336A>C
|
|
|
ENST00000597961.1:c.389A>C
|
ENSP00000472710.1:p.Asn130Thr
|
|
ENST00000598876.1:c.425A>C
|
ENSP00000470533.1:p.Asn142Thr
|
|
ENST00000600281.1:n.439A>C
|
|
|
NM_000528.3:c.398A>C
|
NP_000519.2:p.Asn133Thr
|
|
NM_001173498.1:c.398A>C
|
NP_001166969.1:p.Asn133Thr
|
|
XM_005259913.1:c.398A>C
|
XP_005259970.1:p.Asn133Thr
|
|
XM_005259913.2:c.398A>C
|
XP_005259970.1:p.Asn133Thr
|
|
XM_024451518.1:c.-621A>C
|
XP_024307286.1:n.-621A>C
|
|
NM_000528.4:c.398A>C
MANE Select
|
NP_000519.2:p.Asn133Thr
|
|
NM_001173498.2:c.398A>C
|
NP_001166969.1:p.Asn133Thr
|
|