ENST00000389048.8:c.3590A>T
MANE Select
|
ENSP00000373700.3:p.Glu1197Val
|
|
ENST00000431873.6:c.817A>T
|
|
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ENST00000638605.1:n.467A>T
|
|
|
ENST00000642122.1:c.386A>T
|
ENSP00000493203.1:p.Glu129Val
|
|
ENST00000389048.7:c.3590A>T
|
ENSP00000373700.3:p.Glu1197Val
|
|
ENST00000431873.5:c.470A>T
|
ENSP00000414027.2:p.Glu157Val
|
|
ENST00000618119.4:c.2459A>T
|
ENSP00000482733.1:p.Glu820Val
|
|
NM_004304.4:c.3590A>T
|
NP_004295.2:p.Glu1197Val
|
|
NM_001353765.1:c.386A>T
|
NP_001340694.1:p.Glu129Val
|
|
XM_024452778.1:c.743A>T
|
XP_024308546.1:p.Glu248Val
|
|
XM_024452779.1:c.386A>T
|
XP_024308547.1:p.Glu129Val
|
|
NM_004304.5:c.3590A>T
MANE Select
|
NP_004295.2:p.Glu1197Val
|
|
NM_001353765.2:c.386A>T
|
NP_001340694.1:p.Glu129Val
|
|