ENST00000697124.1:n.738G>T
|
|
|
ENST00000219596.6:c.1617G>T
MANE Select
|
ENSP00000219596.1:p.Lys539Asn
|
|
ENST00000219596.5:c.1617G>T
|
ENSP00000219596.1:p.Lys539Asn
|
|
ENST00000339854.8:c.1077G>T
|
ENSP00000339639.4:p.Lys359Asn
|
|
ENST00000536379.5:c.984G>T
|
ENSP00000445079.1:p.Lys328Asn
|
|
ENST00000536980.5:c.984G>T
|
ENSP00000444178.1:p.Lys328Asn
|
|
ENST00000537682.5:c.1617G>T
|
ENSP00000438611.1:p.Lys539Asn
|
|
ENST00000538326.5:c.*242G>T
|
ENSP00000437486.1:n.*242G>T
|
|
ENST00000539145.5:c.538G>T
|
ENSP00000444471.1:n.538G>T
|
|
ENST00000541159.5:c.984G>T
|
ENSP00000438711.1:p.Lys328Asn
|
|
ENST00000542898.5:c.1710G>T
|
ENSP00000444615.1:p.Lys570Asn
|
|
ENST00000570511.5:c.1165-690G>T
|
ENSP00000458312.1:n.1165-690G>T
|
|
ENST00000572244.5:c.307G>T
|
ENSP00000461186.1:n.307G>T
|
|
ENST00000574583.5:c.532-690G>T
|
ENSP00000460269.1:n.532-690G>T
|
|
ENST00000576315.5:c.532-296G>T
|
ENSP00000460551.1:n.532-296G>T
|
|
ENST00000621655.1:c.984G>T
|
ENSP00000481436.1:p.Lys328Asn
|
|
NM_000243.2:c.1617G>T , LRG_190t1:c.1617G>T
|
NP_000234.1:p.Lys539Asn
|
|
NM_001198536.1:c.984G>T
|
NP_001185465.1:p.Lys328Asn
|
|
XM_017023236.2:c.1614G>T
|
XP_016878725.1:p.Lys538Asn
|
|
XR_001751903.1:n.1806G>T
|
|
|
NM_000243.3:c.1617G>T
MANE Select
|
NP_000234.1:p.Lys539Asn
|
|
NM_001198536.2:c.984G>T
|
NP_001185465.2:p.Lys328Asn
|
|