ENST00000344419.8:c.241T>C
MANE Select
|
ENSP00000343763.4:p.Tyr81His
|
|
ENST00000229447.9:c.241T>C
|
ENSP00000229447.5:p.Tyr81His
|
|
ENST00000344419.7:c.241T>C
|
ENSP00000343763.3:p.Tyr81His
|
|
ENST00000367335.7:c.241T>C
|
ENSP00000356304.3:p.Tyr81His
|
|
ENST00000392255.7:c.241T>C
|
ENSP00000376084.3:p.Tyr81His
|
|
ENST00000392256.6:c.241T>C
|
ENSP00000376085.2:p.Tyr81His
|
|
ENST00000422583.2:c.118T>C
|
ENSP00000397342.2:p.Tyr40His
|
|
ENST00000425615.3:c.76T>C
|
ENSP00000390081.3:p.Tyr26His
|
|
ENST00000500320.7:c.241T>C
|
ENSP00000441276.1:p.Tyr81His
|
|
ENST00000546121.1:n.184T>C
|
|
|
NM_001164694.1:c.241T>C
|
NP_001158166.1:p.Tyr81His
|
|
NM_001164695.1:c.241T>C
|
NP_001158167.1:p.Tyr81His
|
|
NM_203395.2:c.241T>C
|
NP_981932.1:p.Tyr81His
|
|
XM_006715478.2:c.241T>C
|
XP_006715541.1:p.Tyr81His
|
|
XM_006715479.2:c.76T>C
|
XP_006715542.1:p.Tyr26His
|
|
XR_245516.3:n.404T>C
|
|
|
NM_001318495.1:c.63T>C
|
NP_001305424.1:p.Thr21=
|
|
NR_134655.1:n.381T>C
|
|
|
XM_006715478.3:c.241T>C
|
XP_006715541.1:p.Tyr81His
|
|
XM_006715479.3:c.76T>C
|
XP_006715542.1:p.Tyr26His
|
|
NM_001164694.2:c.241T>C
|
NP_001158166.1:p.Tyr81His
|
|
NM_001164695.2:c.241T>C
|
NP_001158167.1:p.Tyr81His
|
|
NM_001318495.2:c.63T>C
|
NP_001305424.1:p.Thr21=
|
|
NM_203395.3:c.241T>C
MANE Select
|
NP_981932.1:p.Tyr81His
|
|
NR_134655.2:n.261T>C
|
|
|