ENST00000455537.7:c.754G>A
MANE Select
|
ENSP00000408979.2:p.Ala252Thr
|
|
ENST00000674619.1:c.754G>A
|
ENSP00000502270.1:p.Ala252Thr
|
|
ENST00000676457.1:c.649G>A
|
ENSP00000501588.1:p.Ala217Thr
|
|
ENST00000286452.5:c.487G>A
|
ENSP00000286452.5:p.Ala163Thr
|
|
ENST00000455537.6:c.754G>A
|
ENSP00000408979.2:p.Ala252Thr
|
|
NM_004984.2:c.754G>A
|
NP_004975.2:p.Ala252Thr
|
|
NM_001354705.1:c.487G>A
|
NP_001341634.1:p.Ala163Thr
|
|
NM_004984.3:c.754G>A
|
NP_004975.2:p.Ala252Thr
|
|
XR_002957324.1:n.987G>A
|
|
|
NM_004984.4:c.754G>A
MANE Select
|
NP_004975.2:p.Ala252Thr
|
|
NM_001354705.2:c.487G>A
|
NP_001341634.1:p.Ala163Thr
|
|