ENST00000409052.6:c.423G>A
|
ENSP00000387210.1:p.Glu141=
|
|
ENST00000696879.1:c.423G>A
|
ENSP00000512947.1:p.Glu141=
|
|
ENST00000696880.1:c.423G>A
|
ENSP00000512948.1:p.Glu141=
|
|
ENST00000696881.1:c.423G>A
|
ENSP00000512949.1:p.Glu141=
|
|
ENST00000696882.1:c.*295G>A
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ENSP00000512950.1:n.*295G>A
|
|
ENST00000696883.1:n.470G>A
|
|
|
ENST00000409930.4:c.525G>A
MANE Select
|
ENSP00000387173.3:p.Glu175=
|
|
ENST00000259206.9:c.534G>A
|
ENSP00000259206.5:p.Glu178=
|
|
ENST00000354115.6:c.471G>A
|
ENSP00000329072.3:p.Glu157=
|
|
ENST00000361779.7:c.423G>A
|
ENSP00000354816.3:p.Glu141=
|
|
ENST00000409052.5:c.423G>A
|
ENSP00000387210.1:p.Glu141=
|
|
ENST00000409930.3:c.525G>A
|
ENSP00000387173.3:p.Glu175=
|
|
NM_000577.4:c.471G>A
|
NP_000568.1:p.Glu157=
|
|
NM_173841.2:c.534G>A , LRG_188t1:c.534G>A
|
NP_776213.1:p.Glu178=
|
|
NM_173842.2:c.525G>A
|
NP_776214.1:p.Glu175=
|
|
NM_173843.2:c.423G>A
|
NP_776215.1:p.Glu141=
|
|
XM_005263661.3:c.423G>A
|
XP_005263718.1:p.Glu141=
|
|
XM_006712497.2:c.423G>A
|
XP_006712560.1:p.Glu141=
|
|
XM_011511121.1:c.423G>A
|
XP_011509423.1:p.Glu141=
|
|
NM_001318914.1:c.423G>A
|
NP_001305843.1:p.Glu141=
|
|
XM_005263661.4:c.423G>A
|
XP_005263718.1:p.Glu141=
|
|
NM_000577.5:c.471G>A
|
NP_000568.1:p.Glu157=
|
|
NM_001318914.2:c.423G>A
|
NP_001305843.1:p.Glu141=
|
|
NM_173842.3:c.525G>A
MANE Select
|
NP_776214.1:p.Glu175=
|
|
NM_173843.3:c.423G>A
|
NP_776215.1:p.Glu141=
|
|
NM_001379360.1:c.423G>A
|
NP_001366289.1:p.Glu141=
|
|
NM_173841.3:c.534G>A
|
NP_776213.1:p.Glu178=
|
|