ENST00000561667.2:c.*2012G>T
|
ENSP00000512522.1:n.*2012G>T
|
|
ENST00000564475.6:c.3534G>T
|
ENSP00000454977.2:p.Glu1178Asp
|
|
ENST00000567510.2:c.2104G>T
|
ENSP00000455969.1:n.2104G>T
|
|
ENST00000568369.6:c.3534G>T
|
ENSP00000456829.1:p.Glu1178Asp
|
|
ENST00000568983.6:n.553G>T
|
|
|
ENST00000696274.1:n.3495G>T
|
|
|
ENST00000696275.1:c.*2769G>T
|
ENSP00000512517.1:n.*2769G>T
|
|
ENST00000696286.1:c.3534G>T
|
ENSP00000512523.1:p.Glu1178Asp
|
|
ENST00000696287.1:c.3405G>T
|
ENSP00000512524.1:p.Glu1135Asp
|
|
ENST00000696291.1:c.*2966G>T
|
ENSP00000512530.1:n.*2966G>T
|
|
ENST00000389301.8:c.3534G>T
MANE Select
|
ENSP00000373952.3:p.Glu1178Asp
|
|
ENST00000305699.15:n.777G>T
|
|
|
ENST00000389301.7:c.3534G>T
|
ENSP00000373952.3:p.Glu1178Asp
|
|
ENST00000561660.1:c.738G>T
|
|
|
ENST00000567879.5:c.12G>T
|
ENSP00000457006.1:p.Glu4Asp
|
|
ENST00000567988.5:c.786G>T
|
|
|
ENST00000568369.5:c.3534G>T
|
ENSP00000456829.1:p.Glu1178Asp
|
|
ENST00000568626.1:c.382G>T
|
|
|
ENST00000568983.5:n.362G>T
|
|
|
NM_000135.2:c.3534G>T , LRG_495t1:c.3534G>T
|
NP_000126.2:p.Glu1178Asp
|
|
NM_001286167.1:c.3534G>T
|
NP_001273096.1:p.Glu1178Asp
|
|
XM_005256294.3:c.3534G>T
|
XP_005256351.1:p.Glu1178Asp
|
|
XM_011522945.1:c.3405G>T
|
XP_011521247.1:p.Glu1135Asp
|
|
XM_011522946.1:c.2511G>T
|
XP_011521248.1:p.Glu837Asp
|
|
XM_011522947.1:c.2511G>T
|
XP_011521249.1:p.Glu837Asp
|
|
XR_933244.1:n.3577G>T
|
|
|
XR_933245.1:n.3577G>T
|
|
|
XR_933246.1:n.3404G>T
|
|
|
NM_000135.3:c.3534G>T
|
NP_000126.2:p.Glu1178Asp
|
|
NM_001286167.2:c.3534G>T
|
NP_001273096.1:p.Glu1178Asp
|
|
XM_005256294.4:c.3534G>T
|
XP_005256351.1:p.Glu1178Asp
|
|
XM_011522945.2:c.3405G>T
|
XP_011521247.1:p.Glu1135Asp
|
|
XM_011522946.3:c.2511G>T
|
XP_011521248.1:p.Glu837Asp
|
|
XM_011522947.2:c.2511G>T
|
XP_011521249.1:p.Glu837Asp
|
|
XM_017023044.2:c.3405G>T
|
XP_016878533.1:p.Glu1135Asp
|
|
XM_024450189.1:c.2511G>T
|
XP_024305957.1:p.Glu837Asp
|
|
XR_001751866.1:n.3404G>T
|
|
|
XR_933244.2:n.3577G>T
|
|
|
XR_933245.2:n.3577G>T
|
|
|
NM_000135.4:c.3534G>T
MANE Select
|
NP_000126.2:p.Glu1178Asp
|
|
NM_001286167.3:c.3534G>T
|
NP_001273096.1:p.Glu1178Asp
|
|