ENST00000697124.1:n.1425T>G
|
|
|
ENST00000219596.6:c.2304T>G
MANE Select
|
ENSP00000219596.1:p.Ala768=
|
|
ENST00000219596.5:c.2304T>G
|
ENSP00000219596.1:p.Ala768=
|
|
ENST00000339854.8:c.1764T>G
|
ENSP00000339639.4:p.Ala588=
|
|
ENST00000536379.5:c.1671T>G
|
ENSP00000445079.1:p.Ala557=
|
|
ENST00000536980.5:c.*580T>G
|
ENSP00000444178.1:n.*580T>G
|
|
ENST00000537682.5:c.*580T>G
|
ENSP00000438611.1:n.*580T>G
|
|
ENST00000538326.5:c.*929T>G
|
ENSP00000437486.1:n.*929T>G
|
|
ENST00000539145.5:c.1225T>G
|
ENSP00000444471.1:n.1225T>G
|
|
ENST00000541159.5:c.1846T>G
|
ENSP00000438711.1:n.1846T>G
|
|
ENST00000542898.5:c.*580T>G
|
ENSP00000444615.1:n.*580T>G
|
|
ENST00000570511.5:c.1709T>G
|
ENSP00000458312.1:n.1709T>G
|
|
ENST00000572244.5:c.994T>G
|
ENSP00000461186.1:n.994T>G
|
|
ENST00000574583.5:c.1076T>G
|
ENSP00000460269.1:n.1076T>G
|
|
ENST00000576315.5:c.1109T>G
|
ENSP00000460551.1:n.1109T>G
|
|
ENST00000621655.1:c.1841T>G
|
ENSP00000481436.1:n.1841T>G
|
|
NM_000243.2:c.2304T>G , LRG_190t1:c.2304T>G
|
NP_000234.1:p.Ala768=
|
|
NM_001198536.1:c.*508T>G
|
NP_001185465.1:n.*508T>G
|
|
XM_017023236.2:c.2301T>G
|
XP_016878725.1:p.Ala767=
|
|
NM_000243.3:c.2304T>G
MANE Select
|
NP_000234.1:p.Ala768=
|
|
NM_001198536.2:c.*508T>G
|
NP_001185465.2:n.*508T>G
|
|