ENST00000697124.1:n.1152A>T
|
|
|
ENST00000219596.6:c.2031A>T
MANE Select
|
ENSP00000219596.1:p.Lys677Asn
|
|
ENST00000219596.5:c.2031A>T
|
ENSP00000219596.1:p.Lys677Asn
|
|
ENST00000339854.8:c.1491A>T
|
ENSP00000339639.4:p.Lys497Asn
|
|
ENST00000536379.5:c.1398A>T
|
ENSP00000445079.1:p.Lys466Asn
|
|
ENST00000536980.5:c.*307A>T
|
ENSP00000444178.1:n.*307A>T
|
|
ENST00000537682.5:c.*307A>T
|
ENSP00000438611.1:n.*307A>T
|
|
ENST00000538326.5:c.*656A>T
|
ENSP00000437486.1:n.*656A>T
|
|
ENST00000539145.5:c.952A>T
|
ENSP00000444471.1:n.952A>T
|
|
ENST00000541159.5:c.1573A>T
|
ENSP00000438711.1:n.1573A>T
|
|
ENST00000542898.5:c.*307A>T
|
ENSP00000444615.1:n.*307A>T
|
|
ENST00000570511.5:c.1436A>T
|
ENSP00000458312.1:n.1436A>T
|
|
ENST00000572244.5:c.721A>T
|
ENSP00000461186.1:n.721A>T
|
|
ENST00000574583.5:c.803A>T
|
ENSP00000460269.1:n.803A>T
|
|
ENST00000576315.5:c.836A>T
|
ENSP00000460551.1:n.836A>T
|
|
ENST00000621655.1:c.1568A>T
|
ENSP00000481436.1:n.1568A>T
|
|
NM_000243.2:c.2031A>T , LRG_190t1:c.2031A>T
|
NP_000234.1:p.Lys677Asn
|
|
NM_001198536.1:c.*235A>T
|
NP_001185465.1:n.*235A>T
|
|
XM_017023236.2:c.2028A>T
|
XP_016878725.1:p.Lys676Asn
|
|
NM_000243.3:c.2031A>T
MANE Select
|
NP_000234.1:p.Lys677Asn
|
|
NM_001198536.2:c.*235A>T
|
NP_001185465.2:n.*235A>T
|
|