ENST00000368407.8:c.476A>T
MANE Select
|
ENSP00000357392.3:p.Asp159Val
|
|
ENST00000368406.2:c.410A>T
|
ENSP00000357391.2:p.Asp137Val
|
|
ENST00000368407.7:c.476A>T
|
ENSP00000357392.3:p.Asp159Val
|
|
ENST00000469878.5:n.727A>T
|
|
|
ENST00000474413.5:n.701A>T
|
|
|
ENST00000497282.1:n.519A>T
|
|
|
NM_004428.2:c.476A>T
|
NP_004419.2:p.Asp159Val
|
|
NM_182685.1:c.410A>T
|
NP_872626.1:p.Asp137Val
|
|
XM_005244940.3:c.287A>T
|
XP_005244997.1:p.Asp96Val
|
|
NM_004428.3:c.476A>T
MANE Select
|
NP_004419.2:p.Asp159Val
|
|
NM_182685.2:c.410A>T
|
NP_872626.1:p.Asp137Val
|
|