ENST00000561667.2:c.*2011A>C
|
ENSP00000512522.1:n.*2011A>C
|
|
ENST00000564475.6:c.3533A>C
|
ENSP00000454977.2:p.Glu1178Ala
|
|
ENST00000567510.2:c.2103A>C
|
ENSP00000455969.1:n.2103A>C
|
|
ENST00000568369.6:c.3533A>C
|
ENSP00000456829.1:p.Glu1178Ala
|
|
ENST00000568983.6:n.552A>C
|
|
|
ENST00000696274.1:n.3494A>C
|
|
|
ENST00000696275.1:c.*2768A>C
|
ENSP00000512517.1:n.*2768A>C
|
|
ENST00000696286.1:c.3533A>C
|
ENSP00000512523.1:p.Glu1178Ala
|
|
ENST00000696287.1:c.3404A>C
|
ENSP00000512524.1:p.Glu1135Ala
|
|
ENST00000696291.1:c.*2965A>C
|
ENSP00000512530.1:n.*2965A>C
|
|
ENST00000389301.8:c.3533A>C
MANE Select
|
ENSP00000373952.3:p.Glu1178Ala
|
|
ENST00000305699.15:n.776A>C
|
|
|
ENST00000389301.7:c.3533A>C
|
ENSP00000373952.3:p.Glu1178Ala
|
|
ENST00000561660.1:c.737A>C
|
|
|
ENST00000567879.5:c.11A>C
|
ENSP00000457006.1:p.Glu4Ala
|
|
ENST00000567988.5:c.785A>C
|
|
|
ENST00000568369.5:c.3533A>C
|
ENSP00000456829.1:p.Glu1178Ala
|
|
ENST00000568626.1:c.381A>C
|
|
|
ENST00000568983.5:n.361A>C
|
|
|
NM_000135.2:c.3533A>C , LRG_495t1:c.3533A>C
|
NP_000126.2:p.Glu1178Ala
|
|
NM_001286167.1:c.3533A>C
|
NP_001273096.1:p.Glu1178Ala
|
|
XM_005256294.3:c.3533A>C
|
XP_005256351.1:p.Glu1178Ala
|
|
XM_011522945.1:c.3404A>C
|
XP_011521247.1:p.Glu1135Ala
|
|
XM_011522946.1:c.2510A>C
|
XP_011521248.1:p.Glu837Ala
|
|
XM_011522947.1:c.2510A>C
|
XP_011521249.1:p.Glu837Ala
|
|
XR_933244.1:n.3576A>C
|
|
|
XR_933245.1:n.3576A>C
|
|
|
XR_933246.1:n.3403A>C
|
|
|
NM_000135.3:c.3533A>C
|
NP_000126.2:p.Glu1178Ala
|
|
NM_001286167.2:c.3533A>C
|
NP_001273096.1:p.Glu1178Ala
|
|
XM_005256294.4:c.3533A>C
|
XP_005256351.1:p.Glu1178Ala
|
|
XM_011522945.2:c.3404A>C
|
XP_011521247.1:p.Glu1135Ala
|
|
XM_011522946.3:c.2510A>C
|
XP_011521248.1:p.Glu837Ala
|
|
XM_011522947.2:c.2510A>C
|
XP_011521249.1:p.Glu837Ala
|
|
XM_017023044.2:c.3404A>C
|
XP_016878533.1:p.Glu1135Ala
|
|
XM_024450189.1:c.2510A>C
|
XP_024305957.1:p.Glu837Ala
|
|
XR_001751866.1:n.3403A>C
|
|
|
XR_933244.2:n.3576A>C
|
|
|
XR_933245.2:n.3576A>C
|
|
|
NM_000135.4:c.3533A>C
MANE Select
|
NP_000126.2:p.Glu1178Ala
|
|
NM_001286167.3:c.3533A>C
|
NP_001273096.1:p.Glu1178Ala
|
|