ENST00000388996.10:c.893A=
MANE Select
|
ENSP00000373648.3:p.Glu298=
|
|
ENST00000521134.6:c.533A=
|
ENSP00000429799.1:p.Glu178=
|
|
ENST00000638588.1:c.566A=
|
ENSP00000491940.1:p.Glu189=
|
|
ENST00000639358.1:c.543A=
|
|
|
ENST00000639496.1:c.566A=
|
ENSP00000491165.1:p.Glu189=
|
|
ENST00000388996.8:c.893A=
|
ENSP00000373648.3:p.Glu298=
|
|
ENST00000519445.5:c.893A=
|
ENSP00000428790.1:p.Glu298=
|
|
ENST00000519589.1:n.671A=
|
|
|
ENST00000521134.5:c.533A=
|
ENSP00000429799.1:p.Glu178=
|
|
ENST00000621976.1:c.530A=
|
ENSP00000482510.1:p.Glu177=
|
|
NM_001204824.1:c.533A=
|
NP_001191753.1:p.Glu178=
|
|
NM_004519.3:c.893A=
|
NP_004510.1:p.Glu298=
|
|
XM_005250914.2:c.-264A=
|
XP_005250971.1:n.-264A=
|
|
XM_006716555.2:c.185A=
|
XP_006716618.1:p.Glu62=
|
|
XM_011517026.1:c.533A=
|
XP_011515328.1:p.Glu178=
|
|
XM_005250914.3:c.-264A=
|
XP_005250971.1:n.-264A=
|
|
XM_006716555.3:c.185A=
|
XP_006716618.1:p.Glu62=
|
|
XM_011517026.2:c.533A=
|
XP_011515328.1:p.Glu178=
|
|
XM_017013400.1:c.671A=
|
XP_016868889.1:p.Glu224=
|
|
NM_004519.4:c.893A=
MANE Select
|
NP_004510.1:p.Glu298=
|
|
NM_001204824.2:c.533A=
|
NP_001191753.1:p.Glu178=
|
|