ENST00000389048.8:c.3540T>A
MANE Select
|
ENSP00000373700.3:p.Val1180=
|
|
ENST00000431873.6:c.767T>A
|
|
|
ENST00000638605.1:n.417T>A
|
|
|
ENST00000642122.1:c.336T>A
|
ENSP00000493203.1:p.Val112=
|
|
ENST00000389048.7:c.3540T>A
|
ENSP00000373700.3:p.Val1180=
|
|
ENST00000431873.5:c.420T>A
|
ENSP00000414027.2:p.Val140=
|
|
ENST00000618119.4:c.2409T>A
|
ENSP00000482733.1:p.Val803=
|
|
NM_004304.4:c.3540T>A
|
NP_004295.2:p.Val1180=
|
|
NM_001353765.1:c.336T>A
|
NP_001340694.1:p.Val112=
|
|
XM_024452778.1:c.693T>A
|
XP_024308546.1:p.Val231=
|
|
XM_024452779.1:c.336T>A
|
XP_024308547.1:p.Val112=
|
|
NM_004304.5:c.3540T>A
MANE Select
|
NP_004295.2:p.Val1180=
|
|
NM_001353765.2:c.336T>A
|
NP_001340694.1:p.Val112=
|
|