ENST00000389048.8:c.3512T=
MANE Select
|
ENSP00000373700.3:p.Ile1171=
|
|
ENST00000431873.6:c.739T=
|
|
|
ENST00000638605.1:n.389T=
|
|
|
ENST00000642122.1:c.308T=
|
ENSP00000493203.1:p.Ile103=
|
|
ENST00000389048.7:c.3512T=
|
ENSP00000373700.3:p.Ile1171=
|
|
ENST00000431873.5:c.392T=
|
ENSP00000414027.2:p.Ile131=
|
|
ENST00000453137.1:c.206T=
|
ENSP00000387488.1:p.Ile69=
|
|
ENST00000618119.4:c.2381T=
|
ENSP00000482733.1:p.Ile794=
|
|
NM_004304.4:c.3512T=
|
NP_004295.2:p.Ile1171=
|
|
NM_001353765.1:c.308T=
|
NP_001340694.1:p.Ile103=
|
|
XM_024452778.1:c.665T=
|
XP_024308546.1:p.Ile222=
|
|
XM_024452779.1:c.308T=
|
XP_024308547.1:p.Ile103=
|
|
NM_004304.5:c.3512T=
MANE Select
|
NP_004295.2:p.Ile1171=
|
|
NM_001353765.2:c.308T=
|
NP_001340694.1:p.Ile103=
|
|