ENST00000697124.1:n.1328C>T
|
|
|
ENST00000219596.6:c.2207C>T
MANE Select
|
ENSP00000219596.1:p.Ala736Val
|
|
ENST00000219596.5:c.2207C>T
|
ENSP00000219596.1:p.Ala736Val
|
|
ENST00000339854.8:c.1667C>T
|
ENSP00000339639.4:p.Ala556Val
|
|
ENST00000536379.5:c.1574C>T
|
ENSP00000445079.1:p.Ala525Val
|
|
ENST00000536980.5:c.*483C>T
|
ENSP00000444178.1:n.*483C>T
|
|
ENST00000537682.5:c.*483C>T
|
ENSP00000438611.1:n.*483C>T
|
|
ENST00000538326.5:c.*832C>T
|
ENSP00000437486.1:n.*832C>T
|
|
ENST00000539145.5:c.1128C>T
|
ENSP00000444471.1:n.1128C>T
|
|
ENST00000541159.5:c.1749C>T
|
ENSP00000438711.1:n.1749C>T
|
|
ENST00000542898.5:c.*483C>T
|
ENSP00000444615.1:n.*483C>T
|
|
ENST00000570511.5:c.1612C>T
|
ENSP00000458312.1:n.1612C>T
|
|
ENST00000572244.5:c.897C>T
|
ENSP00000461186.1:n.897C>T
|
|
ENST00000574583.5:c.979C>T
|
ENSP00000460269.1:n.979C>T
|
|
ENST00000576315.5:c.1012C>T
|
ENSP00000460551.1:n.1012C>T
|
|
ENST00000621655.1:c.1744C>T
|
ENSP00000481436.1:n.1744C>T
|
|
NM_000243.2:c.2207C>T , LRG_190t1:c.2207C>T
|
NP_000234.1:p.Ala736Val
|
|
NM_001198536.1:c.*411C>T
|
NP_001185465.1:n.*411C>T
|
|
XM_017023236.2:c.2204C>T
|
XP_016878725.1:p.Ala735Val
|
|
NM_000243.3:c.2207C>T
MANE Select
|
NP_000234.1:p.Ala736Val
|
|
NM_001198536.2:c.*411C>T
|
NP_001185465.2:n.*411C>T
|
|