ENST00000636937.2:c.3472C>G
|
ENSP00000516154.1:p.Leu1158Val
|
|
ENST00000268124.11:c.3472C>G
MANE Select
|
ENSP00000268124.5:p.Leu1158Val
|
|
ENST00000530292.3:c.3073C>G
|
ENSP00000432885.2:p.Leu1025Val
|
|
ENST00000635986.2:c.*542C>G
|
ENSP00000490653.2:n.*542C>G
|
|
ENST00000636774.1:c.*2039C>G
|
ENSP00000489799.1:n.*2039C>G
|
|
ENST00000637238.1:c.2281C>G
|
ENSP00000490756.1:n.2281C>G
|
|
ENST00000637264.1:c.2544C>G
|
|
|
ENST00000666746.1:c.3049C>G
|
|
|
ENST00000672071.1:n.3670C>G
|
|
|
ENST00000672695.1:n.649C>G
|
|
|
ENST00000672923.2:n.3472C>G
|
|
|
ENST00000268124.9:c.3472C>G
|
ENSP00000268124.5:p.Leu1158Val
|
|
ENST00000442287.6:c.3472C>G
|
ENSP00000399851.2:p.Leu1158Val
|
|
ENST00000530292.2:c.556C>G
|
ENSP00000432885.1:p.Leu186Val
|
|
ENST00000631044.2:c.*2896C>G
|
ENSP00000486730.1:n.*2896C>G
|
|
NM_001126131.1:c.3472C>G
|
NP_001119603.1:p.Leu1158Val
|
|
NM_002693.2:c.3472C>G
|
NP_002684.1:p.Leu1158Val
|
|
NM_001126131.2:c.3472C>G
|
NP_001119603.1:p.Leu1158Val
|
|
NM_002693.3:c.3472C>G
MANE Select
|
NP_002684.1:p.Leu1158Val
|
|