ENST00000344419.8:c.366G>A
MANE Select
|
ENSP00000343763.4:p.Thr122=
|
|
ENST00000229447.9:c.366G>A
|
ENSP00000229447.5:p.Thr122=
|
|
ENST00000344419.7:c.366G>A
|
ENSP00000343763.3:p.Thr122=
|
|
ENST00000367335.7:c.366G>A
|
ENSP00000356304.3:p.Thr122=
|
|
ENST00000392255.7:c.366G>A
|
ENSP00000376084.3:p.Thr122=
|
|
ENST00000392256.6:c.366G>A
|
ENSP00000376085.2:p.Thr122=
|
|
ENST00000422583.2:c.179+64G>A
|
ENSP00000397342.2:n.179+64G>A
|
|
ENST00000425615.3:c.201G>A
|
ENSP00000390081.3:p.Thr67=
|
|
ENST00000500320.7:c.366G>A
|
ENSP00000441276.1:p.Thr122=
|
|
ENST00000546121.1:n.309G>A
|
|
|
NM_001164694.1:c.366G>A
|
NP_001158166.1:p.Thr122=
|
|
NM_001164695.1:c.366G>A
|
NP_001158167.1:p.Thr122=
|
|
NM_203395.2:c.366G>A
|
NP_981932.1:p.Thr122=
|
|
XM_006715478.2:c.366G>A
|
XP_006715541.1:p.Thr122=
|
|
XM_006715479.2:c.201G>A
|
XP_006715542.1:p.Thr67=
|
|
XR_245516.3:n.529G>A
|
|
|
NM_001318495.1:c.124+64G>A
|
NP_001305424.1:n.124+64G>A
|
|
NR_134655.1:n.506G>A
|
|
|
XM_006715478.3:c.366G>A
|
XP_006715541.1:p.Thr122=
|
|
XM_006715479.3:c.201G>A
|
XP_006715542.1:p.Thr67=
|
|
NM_001164694.2:c.366G>A
|
NP_001158166.1:p.Thr122=
|
|
NM_001164695.2:c.366G>A
|
NP_001158167.1:p.Thr122=
|
|
NM_001318495.2:c.124+64G>A
|
NP_001305424.1:n.124+64G>A
|
|
NM_203395.3:c.366G>A
MANE Select
|
NP_981932.1:p.Thr122=
|
|
NR_134655.2:n.386G>A
|
|
|