ENST00000252288.8:c.466G>A
MANE Select
|
ENSP00000252288.1:p.Ala156Thr
|
|
ENST00000447102.8:c.466G>A
|
ENSP00000403536.2:p.Ala156Thr
|
|
ENST00000591788.3:c.149G>A
|
|
|
ENST00000640164.1:n.299G>A
|
|
|
ENST00000640762.1:c.397G>A
|
ENSP00000492031.1:p.Ala133Thr
|
|
ENST00000252288.6:c.466G>A
|
ENSP00000252288.1:p.Ala156Thr
|
|
ENST00000447102.7:c.466G>A
|
ENSP00000403536.2:p.Ala156Thr
|
|
ENST00000591788.2:c.151G>A
|
ENSP00000466341.2:p.Ala51Thr
|
|
NM_000156.5:c.466G>A
|
NP_000147.1:p.Ala156Thr
|
|
NM_138924.2:c.466G>A
|
NP_620279.1:p.Ala156Thr
|
|
NM_000156.6:c.466G>A
MANE Select
|
NP_000147.1:p.Ala156Thr
|
|
NM_138924.3:c.466G>A
|
NP_620279.1:p.Ala156Thr
|
|