ENST00000455537.7:c.772T>A
MANE Select
|
ENSP00000408979.2:p.Ser258Thr
|
|
ENST00000674619.1:c.772T>A
|
ENSP00000502270.1:p.Ser258Thr
|
|
ENST00000676457.1:c.667T>A
|
ENSP00000501588.1:p.Ser223Thr
|
|
ENST00000286452.5:c.505T>A
|
ENSP00000286452.5:p.Ser169Thr
|
|
ENST00000455537.6:c.772T>A
|
ENSP00000408979.2:p.Ser258Thr
|
|
NM_004984.2:c.772T>A
|
NP_004975.2:p.Ser258Thr
|
|
NM_001354705.1:c.505T>A
|
NP_001341634.1:p.Ser169Thr
|
|
NM_004984.3:c.772T>A
|
NP_004975.2:p.Ser258Thr
|
|
XR_002957324.1:n.1005T>A
|
|
|
NM_004984.4:c.772T>A
MANE Select
|
NP_004975.2:p.Ser258Thr
|
|
NM_001354705.2:c.505T>A
|
NP_001341634.1:p.Ser169Thr
|
|