ENST00000455537.7:c.704G>T
MANE Select
|
ENSP00000408979.2:p.Gly235Val
|
|
ENST00000674619.1:c.704G>T
|
ENSP00000502270.1:p.Gly235Val
|
|
ENST00000676457.1:c.599G>T
|
ENSP00000501588.1:p.Gly200Val
|
|
ENST00000286452.5:c.437G>T
|
ENSP00000286452.5:p.Gly146Val
|
|
ENST00000455537.6:c.704G>T
|
ENSP00000408979.2:p.Gly235Val
|
|
NM_004984.2:c.704G>T
|
NP_004975.2:p.Gly235Val
|
|
NM_001354705.1:c.437G>T
|
NP_001341634.1:p.Gly146Val
|
|
NM_004984.3:c.704G>T
|
NP_004975.2:p.Gly235Val
|
|
XR_002957324.1:n.937G>T
|
|
|
NM_004984.4:c.704G>T
MANE Select
|
NP_004975.2:p.Gly235Val
|
|
NM_001354705.2:c.437G>T
|
NP_001341634.1:p.Gly146Val
|
|