ENST00000697124.1:n.1412G>A
|
|
|
ENST00000219596.6:c.2291G>A
MANE Select
|
ENSP00000219596.1:p.Gly764Glu
|
|
ENST00000219596.5:c.2291G>A
|
ENSP00000219596.1:p.Gly764Glu
|
|
ENST00000339854.8:c.1751G>A
|
ENSP00000339639.4:p.Gly584Glu
|
|
ENST00000536379.5:c.1658G>A
|
ENSP00000445079.1:p.Gly553Glu
|
|
ENST00000536980.5:c.*567G>A
|
ENSP00000444178.1:n.*567G>A
|
|
ENST00000537682.5:c.*567G>A
|
ENSP00000438611.1:n.*567G>A
|
|
ENST00000538326.5:c.*916G>A
|
ENSP00000437486.1:n.*916G>A
|
|
ENST00000539145.5:c.1212G>A
|
ENSP00000444471.1:n.1212G>A
|
|
ENST00000541159.5:c.1833G>A
|
ENSP00000438711.1:n.1833G>A
|
|
ENST00000542898.5:c.*567G>A
|
ENSP00000444615.1:n.*567G>A
|
|
ENST00000570511.5:c.1696G>A
|
ENSP00000458312.1:n.1696G>A
|
|
ENST00000572244.5:c.981G>A
|
ENSP00000461186.1:n.981G>A
|
|
ENST00000574583.5:c.1063G>A
|
ENSP00000460269.1:n.1063G>A
|
|
ENST00000576315.5:c.1096G>A
|
ENSP00000460551.1:n.1096G>A
|
|
ENST00000621655.1:c.1828G>A
|
ENSP00000481436.1:n.1828G>A
|
|
NM_000243.2:c.2291G>A , LRG_190t1:c.2291G>A
|
NP_000234.1:p.Gly764Glu
|
|
NM_001198536.1:c.*495G>A
|
NP_001185465.1:n.*495G>A
|
|
XM_017023236.2:c.2288G>A
|
XP_016878725.1:p.Gly763Glu
|
|
NM_000243.3:c.2291G>A
MANE Select
|
NP_000234.1:p.Gly764Glu
|
|
NM_001198536.2:c.*495G>A
|
NP_001185465.2:n.*495G>A
|
|