ENST00000697124.1:n.873G>C
|
|
|
ENST00000219596.6:c.1752G>C
MANE Select
|
ENSP00000219596.1:p.Met584Ile
|
|
ENST00000219596.5:c.1752G>C
|
ENSP00000219596.1:p.Met584Ile
|
|
ENST00000339854.8:c.1212G>C
|
ENSP00000339639.4:p.Met404Ile
|
|
ENST00000536379.5:c.1119G>C
|
ENSP00000445079.1:p.Met373Ile
|
|
ENST00000536980.5:c.1119G>C
|
ENSP00000444178.1:p.Met373Ile
|
|
ENST00000537682.5:c.1752G>C
|
ENSP00000438611.1:p.Met584Ile
|
|
ENST00000538326.5:c.*377G>C
|
ENSP00000437486.1:n.*377G>C
|
|
ENST00000539145.5:c.673G>C
|
ENSP00000444471.1:n.673G>C
|
|
ENST00000541159.5:c.1119G>C
|
ENSP00000438711.1:p.Met373Ile
|
|
ENST00000542898.5:c.1845G>C
|
ENSP00000444615.1:p.Met615Ile
|
|
ENST00000570511.5:c.1165-369G>C
|
ENSP00000458312.1:n.1165-369G>C
|
|
ENST00000572244.5:c.442G>C
|
ENSP00000461186.1:n.442G>C
|
|
ENST00000574583.5:c.532-369G>C
|
ENSP00000460269.1:n.532-369G>C
|
|
ENST00000576315.5:c.557G>C
|
ENSP00000460551.1:n.557G>C
|
|
ENST00000621655.1:c.1119G>C
|
ENSP00000481436.1:p.Met373Ile
|
|
NM_000243.2:c.1752G>C , LRG_190t1:c.1752G>C
|
NP_000234.1:p.Met584Ile
|
|
NM_001198536.1:c.1119G>C
|
NP_001185465.1:p.Met373Ile
|
|
XM_017023236.2:c.1749G>C
|
XP_016878725.1:p.Met583Ile
|
|
XR_001751903.1:n.1941G>C
|
|
|
NM_000243.3:c.1752G>C
MANE Select
|
NP_000234.1:p.Met584Ile
|
|
NM_001198536.2:c.1119G>C
|
NP_001185465.2:p.Met373Ile
|
|