ENST00000697124.1:n.1286T>G
|
|
|
ENST00000219596.6:c.2165T>G
MANE Select
|
ENSP00000219596.1:p.Val722Gly
|
|
ENST00000219596.5:c.2165T>G
|
ENSP00000219596.1:p.Val722Gly
|
|
ENST00000339854.8:c.1625T>G
|
ENSP00000339639.4:p.Val542Gly
|
|
ENST00000536379.5:c.1532T>G
|
ENSP00000445079.1:p.Val511Gly
|
|
ENST00000536980.5:c.*441T>G
|
ENSP00000444178.1:n.*441T>G
|
|
ENST00000537682.5:c.*441T>G
|
ENSP00000438611.1:n.*441T>G
|
|
ENST00000538326.5:c.*790T>G
|
ENSP00000437486.1:n.*790T>G
|
|
ENST00000539145.5:c.1086T>G
|
ENSP00000444471.1:n.1086T>G
|
|
ENST00000541159.5:c.1707T>G
|
ENSP00000438711.1:n.1707T>G
|
|
ENST00000542898.5:c.*441T>G
|
ENSP00000444615.1:n.*441T>G
|
|
ENST00000570511.5:c.1570T>G
|
ENSP00000458312.1:n.1570T>G
|
|
ENST00000572244.5:c.855T>G
|
ENSP00000461186.1:n.855T>G
|
|
ENST00000574583.5:c.937T>G
|
ENSP00000460269.1:n.937T>G
|
|
ENST00000576315.5:c.970T>G
|
ENSP00000460551.1:n.970T>G
|
|
ENST00000621655.1:c.1702T>G
|
ENSP00000481436.1:n.1702T>G
|
|
NM_000243.2:c.2165T>G , LRG_190t1:c.2165T>G
|
NP_000234.1:p.Val722Gly
|
|
NM_001198536.1:c.*369T>G
|
NP_001185465.1:n.*369T>G
|
|
XM_017023236.2:c.2162T>G
|
XP_016878725.1:p.Val721Gly
|
|
NM_000243.3:c.2165T>G
MANE Select
|
NP_000234.1:p.Val722Gly
|
|
NM_001198536.2:c.*369T>G
|
NP_001185465.2:n.*369T>G
|
|