ENST00000389048.8:c.3500A>T
MANE Select
|
ENSP00000373700.3:p.Glu1167Val
|
|
ENST00000431873.6:c.727A>T
|
|
|
ENST00000638605.1:n.377A>T
|
|
|
ENST00000642122.1:c.296A>T
|
ENSP00000493203.1:p.Glu99Val
|
|
ENST00000389048.7:c.3500A>T
|
ENSP00000373700.3:p.Glu1167Val
|
|
ENST00000431873.5:c.380A>T
|
ENSP00000414027.2:p.Glu127Val
|
|
ENST00000453137.1:c.194A>T
|
ENSP00000387488.1:p.Glu65Val
|
|
ENST00000618119.4:c.2369A>T
|
ENSP00000482733.1:p.Glu790Val
|
|
NM_004304.4:c.3500A>T
|
NP_004295.2:p.Glu1167Val
|
|
NM_001353765.1:c.296A>T
|
NP_001340694.1:p.Glu99Val
|
|
XM_024452778.1:c.653A>T
|
XP_024308546.1:p.Glu218Val
|
|
XM_024452779.1:c.296A>T
|
XP_024308547.1:p.Glu99Val
|
|
NM_004304.5:c.3500A>T
MANE Select
|
NP_004295.2:p.Glu1167Val
|
|
NM_001353765.2:c.296A>T
|
NP_001340694.1:p.Glu99Val
|
|