ENST00000328194.8:c.3564G>A
MANE Select
|
ENSP00000328524.3:p.Glu1188=
|
|
ENST00000525784.6:n.1426G>A
|
|
|
ENST00000530780.2:c.*3390G>A
|
ENSP00000433925.1:n.*3390G>A
|
|
ENST00000531747.2:n.3235G>A
|
|
|
ENST00000679446.1:n.3485G>A
|
|
|
ENST00000679458.1:n.4965G>A
|
|
|
ENST00000679460.1:n.4626G>A
|
|
|
ENST00000679568.1:c.3564G>A
|
ENSP00000505860.1:p.Glu1188=
|
|
ENST00000679745.1:n.4069G>A
|
|
|
ENST00000679773.1:n.2725G>A
|
|
|
ENST00000679926.1:n.4866G>A
|
|
|
ENST00000679999.1:c.*621G>A
|
ENSP00000505198.1:n.*621G>A
|
|
ENST00000680252.1:c.3231G>A
|
|
|
ENST00000680294.1:c.3357G>A
|
ENSP00000506113.1:p.Glu1119=
|
|
ENST00000680358.1:n.2863G>A
|
|
|
ENST00000680470.1:c.*1345G>A
|
ENSP00000505975.1:n.*1345G>A
|
|
ENST00000680554.1:c.*97G>A
|
ENSP00000505621.1:n.*97G>A
|
|
ENST00000680576.1:n.5040G>A
|
|
|
ENST00000680599.1:n.3605G>A
|
|
|
ENST00000680742.1:c.*97G>A
|
ENSP00000505206.1:n.*97G>A
|
|
ENST00000680791.1:n.2448G>A
|
|
|
ENST00000680885.1:n.5266G>A
|
|
|
ENST00000681158.1:c.3148G>A
|
|
|
ENST00000681203.1:c.3492G>A
|
ENSP00000506456.1:p.Glu1164=
|
|
ENST00000681371.1:n.3436G>A
|
|
|
ENST00000681425.1:n.4042G>A
|
|
|
ENST00000681639.1:n.1843G>A
|
|
|
ENST00000328194.7:c.3564G>A
|
ENSP00000328524.3:p.Glu1188=
|
|
ENST00000525784.5:c.500G>A
|
|
|
ENST00000527700.5:n.3126G>A
|
|
|
ENST00000528725.5:c.260G>A
|
|
|
ENST00000529977.5:n.1465G>A
|
|
|
ENST00000530044.5:c.3564G>A
|
ENSP00000435866.1:p.Glu1188=
|
|
ENST00000531747.1:c.800G>A
|
|
|
ENST00000533737.5:c.227G>A
|
|
|
NM_001243254.1:c.3564G>A
|
NP_001230183.1:p.Glu1188=
|
|
NM_015213.3:c.3564G>A
|
NP_056028.2:p.Glu1188=
|
|
XM_005252832.1:c.3564G>A
|
XP_005252889.1:p.Glu1188=
|
|
XM_011519952.1:c.3564G>A
|
XP_011518254.1:p.Glu1188=
|
|
XM_011519953.1:c.1662G>A
|
XP_011518255.1:p.Glu554=
|
|
XR_242782.2:n.3746G>A
|
|
|
XR_930851.1:n.3746G>A
|
|
|
NM_001348749.1:c.3492G>A
|
NP_001335678.1:p.Glu1164=
|
|
NM_001348750.1:c.3276G>A
|
NP_001335679.1:p.Glu1092=
|
|
NR_145966.2:n.3738G>A
|
|
|
NM_015213.4:c.3564G>A
MANE Select
|
NP_056028.2:p.Glu1188=
|
|
NM_001243254.2:c.3564G>A
|
NP_001230183.1:p.Glu1188=
|
|
NM_001348749.2:c.3492G>A
|
NP_001335678.1:p.Glu1164=
|
|
NM_001348750.2:c.3276G>A
|
NP_001335679.1:p.Glu1092=
|
|