ENST00000299314.12:c.3590A>T
MANE Select
|
ENSP00000299314.7:p.Glu1197Val
|
|
ENST00000299314.11:c.3590A>T
|
ENSP00000299314.7:p.Glu1197Val
|
|
ENST00000549738.5:c.488A>T
|
ENSP00000450161.1:n.488A>T
|
|
NM_024312.4:c.3590A>T
|
NP_077288.2:p.Glu1197Val
|
|
XM_011538731.1:c.3509A>T
|
XP_011537033.1:p.Glu1170Val
|
|
XM_011538731.2:c.3509A>T
|
XP_011537033.1:p.Glu1170Val
|
|
XM_017019961.1:c.3374A>T
|
XP_016875450.1:p.Glu1125Val
|
|
XM_017019962.2:c.2363A>T
|
XP_016875451.1:p.Glu788Val
|
|
NM_024312.5:c.3590A>T
MANE Select
|
NP_077288.2:p.Glu1197Val
|
|