ENST00000697124.1:n.1307T>G
|
|
|
ENST00000219596.6:c.2186T>G
MANE Select
|
ENSP00000219596.1:p.Ile729Ser
|
|
ENST00000219596.5:c.2186T>G
|
ENSP00000219596.1:p.Ile729Ser
|
|
ENST00000339854.8:c.1646T>G
|
ENSP00000339639.4:p.Ile549Ser
|
|
ENST00000536379.5:c.1553T>G
|
ENSP00000445079.1:p.Ile518Ser
|
|
ENST00000536980.5:c.*462T>G
|
ENSP00000444178.1:n.*462T>G
|
|
ENST00000537682.5:c.*462T>G
|
ENSP00000438611.1:n.*462T>G
|
|
ENST00000538326.5:c.*811T>G
|
ENSP00000437486.1:n.*811T>G
|
|
ENST00000539145.5:c.1107T>G
|
ENSP00000444471.1:n.1107T>G
|
|
ENST00000541159.5:c.1728T>G
|
ENSP00000438711.1:n.1728T>G
|
|
ENST00000542898.5:c.*462T>G
|
ENSP00000444615.1:n.*462T>G
|
|
ENST00000570511.5:c.1591T>G
|
ENSP00000458312.1:n.1591T>G
|
|
ENST00000572244.5:c.876T>G
|
ENSP00000461186.1:n.876T>G
|
|
ENST00000574583.5:c.958T>G
|
ENSP00000460269.1:n.958T>G
|
|
ENST00000576315.5:c.991T>G
|
ENSP00000460551.1:n.991T>G
|
|
ENST00000621655.1:c.1723T>G
|
ENSP00000481436.1:n.1723T>G
|
|
NM_000243.2:c.2186T>G , LRG_190t1:c.2186T>G
|
NP_000234.1:p.Ile729Ser
|
|
NM_001198536.1:c.*390T>G
|
NP_001185465.1:n.*390T>G
|
|
XM_017023236.2:c.2183T>G
|
XP_016878725.1:p.Ile728Ser
|
|
NM_000243.3:c.2186T>G
MANE Select
|
NP_000234.1:p.Ile729Ser
|
|
NM_001198536.2:c.*390T>G
|
NP_001185465.2:n.*390T>G
|
|