ENST00000697124.1:n.1179T>A
|
|
|
ENST00000219596.6:c.2058T>A
MANE Select
|
ENSP00000219596.1:p.Asn686Lys
|
|
ENST00000219596.5:c.2058T>A
|
ENSP00000219596.1:p.Asn686Lys
|
|
ENST00000339854.8:c.1518T>A
|
ENSP00000339639.4:p.Asn506Lys
|
|
ENST00000536379.5:c.1425T>A
|
ENSP00000445079.1:p.Asn475Lys
|
|
ENST00000536980.5:c.*334T>A
|
ENSP00000444178.1:n.*334T>A
|
|
ENST00000537682.5:c.*334T>A
|
ENSP00000438611.1:n.*334T>A
|
|
ENST00000538326.5:c.*683T>A
|
ENSP00000437486.1:n.*683T>A
|
|
ENST00000539145.5:c.979T>A
|
ENSP00000444471.1:n.979T>A
|
|
ENST00000541159.5:c.1600T>A
|
ENSP00000438711.1:n.1600T>A
|
|
ENST00000542898.5:c.*334T>A
|
ENSP00000444615.1:n.*334T>A
|
|
ENST00000570511.5:c.1463T>A
|
ENSP00000458312.1:n.1463T>A
|
|
ENST00000572244.5:c.748T>A
|
ENSP00000461186.1:n.748T>A
|
|
ENST00000574583.5:c.830T>A
|
ENSP00000460269.1:n.830T>A
|
|
ENST00000576315.5:c.863T>A
|
ENSP00000460551.1:n.863T>A
|
|
ENST00000621655.1:c.1595T>A
|
ENSP00000481436.1:n.1595T>A
|
|
NM_000243.2:c.2058T>A , LRG_190t1:c.2058T>A
|
NP_000234.1:p.Asn686Lys
|
|
NM_001198536.1:c.*262T>A
|
NP_001185465.1:n.*262T>A
|
|
XM_017023236.2:c.2055T>A
|
XP_016878725.1:p.Asn685Lys
|
|
NM_000243.3:c.2058T>A
MANE Select
|
NP_000234.1:p.Asn686Lys
|
|
NM_001198536.2:c.*262T>A
|
NP_001185465.2:n.*262T>A
|
|