ENST00000295897.9:c.1084C>A
MANE Select
|
ENSP00000295897.4:p.His362Asn
|
|
ENST00000295897.8:c.1084C>A
|
ENSP00000295897.4:p.His362Asn
|
|
ENST00000401494.7:c.739C>A
|
ENSP00000384695.3:p.His247Asn
|
|
ENST00000415165.6:c.508C>A
|
ENSP00000401820.2:p.His170Asn
|
|
ENST00000476441.6:c.*363C>A
|
ENSP00000423727.1:n.*363C>A
|
|
ENST00000484992.1:n.404C>A
|
|
|
ENST00000503124.5:c.634C>A
|
ENSP00000421027.1:p.His212Asn
|
|
ENST00000504043.1:n.87C>A
|
|
|
ENST00000505649.5:n.770C>A
|
|
|
ENST00000509063.5:c.1084C>A
|
ENSP00000422784.1:p.His362Asn
|
|
ENST00000511370.1:c.617C>A
|
|
|
ENST00000621085.4:c.491-46C>A
|
ENSP00000483421.1:n.491-46C>A
|
|
ENST00000621628.4:c.487-42C>A
|
ENSP00000480485.1:n.487-42C>A
|
|
NM_000477.5:c.1084C>A
|
NP_000468.1:p.His362Asn
|
|
NM_000477.6:c.1084C>A
|
NP_000468.1:p.His362Asn
|
|
NM_000477.7:c.1084C>A
MANE Select
|
NP_000468.1:p.His362Asn
|
|