ENST00000697124.1:n.1415A>C
|
|
|
ENST00000219596.6:c.2294A>C
MANE Select
|
ENSP00000219596.1:p.Lys765Thr
|
|
ENST00000219596.5:c.2294A>C
|
ENSP00000219596.1:p.Lys765Thr
|
|
ENST00000339854.8:c.1754A>C
|
ENSP00000339639.4:p.Lys585Thr
|
|
ENST00000536379.5:c.1661A>C
|
ENSP00000445079.1:p.Lys554Thr
|
|
ENST00000536980.5:c.*570A>C
|
ENSP00000444178.1:n.*570A>C
|
|
ENST00000537682.5:c.*570A>C
|
ENSP00000438611.1:n.*570A>C
|
|
ENST00000538326.5:c.*919A>C
|
ENSP00000437486.1:n.*919A>C
|
|
ENST00000539145.5:c.1215A>C
|
ENSP00000444471.1:n.1215A>C
|
|
ENST00000541159.5:c.1836A>C
|
ENSP00000438711.1:n.1836A>C
|
|
ENST00000542898.5:c.*570A>C
|
ENSP00000444615.1:n.*570A>C
|
|
ENST00000570511.5:c.1699A>C
|
ENSP00000458312.1:n.1699A>C
|
|
ENST00000572244.5:c.984A>C
|
ENSP00000461186.1:n.984A>C
|
|
ENST00000574583.5:c.1066A>C
|
ENSP00000460269.1:n.1066A>C
|
|
ENST00000576315.5:c.1099A>C
|
ENSP00000460551.1:n.1099A>C
|
|
ENST00000621655.1:c.1831A>C
|
ENSP00000481436.1:n.1831A>C
|
|
NM_000243.2:c.2294A>C , LRG_190t1:c.2294A>C
|
NP_000234.1:p.Lys765Thr
|
|
NM_001198536.1:c.*498A>C
|
NP_001185465.1:n.*498A>C
|
|
XM_017023236.2:c.2291A>C
|
XP_016878725.1:p.Lys764Thr
|
|
NM_000243.3:c.2294A>C
MANE Select
|
NP_000234.1:p.Lys765Thr
|
|
NM_001198536.2:c.*498A>C
|
NP_001185465.2:n.*498A>C
|
|