ENST00000697124.1:n.1043T>G
|
|
|
ENST00000219596.6:c.1922T>G
MANE Select
|
ENSP00000219596.1:p.Ile641Ser
|
|
ENST00000219596.5:c.1922T>G
|
ENSP00000219596.1:p.Ile641Ser
|
|
ENST00000339854.8:c.1382T>G
|
ENSP00000339639.4:p.Ile461Ser
|
|
ENST00000536379.5:c.1289T>G
|
ENSP00000445079.1:p.Ile430Ser
|
|
ENST00000536980.5:c.*198T>G
|
ENSP00000444178.1:n.*198T>G
|
|
ENST00000537682.5:c.*198T>G
|
ENSP00000438611.1:n.*198T>G
|
|
ENST00000538326.5:c.*547T>G
|
ENSP00000437486.1:n.*547T>G
|
|
ENST00000539145.5:c.843T>G
|
ENSP00000444471.1:n.843T>G
|
|
ENST00000541159.5:c.1464T>G
|
ENSP00000438711.1:n.1464T>G
|
|
ENST00000542898.5:c.*198T>G
|
ENSP00000444615.1:n.*198T>G
|
|
ENST00000570511.5:c.1327T>G
|
ENSP00000458312.1:n.1327T>G
|
|
ENST00000572244.5:c.612T>G
|
ENSP00000461186.1:n.612T>G
|
|
ENST00000574583.5:c.694T>G
|
ENSP00000460269.1:n.694T>G
|
|
ENST00000576315.5:c.727T>G
|
ENSP00000460551.1:n.727T>G
|
|
ENST00000621655.1:c.1459T>G
|
ENSP00000481436.1:n.1459T>G
|
|
NM_000243.2:c.1922T>G , LRG_190t1:c.1922T>G
|
NP_000234.1:p.Ile641Ser
|
|
NM_001198536.1:c.*126T>G
|
NP_001185465.1:n.*126T>G
|
|
XM_017023236.2:c.1919T>G
|
XP_016878725.1:p.Ile640Ser
|
|
NM_000243.3:c.1922T>G
MANE Select
|
NP_000234.1:p.Ile641Ser
|
|
NM_001198536.2:c.*126T>G
|
NP_001185465.2:n.*126T>G
|
|