ENST00000299314.12:c.1346A>T
MANE Select
|
ENSP00000299314.7:p.Asp449Val
|
|
ENST00000299314.11:c.1346A>T
|
ENSP00000299314.7:p.Asp449Val
|
|
ENST00000549940.5:c.1346A>T
|
ENSP00000449150.1:p.Asp449Val
|
|
ENST00000552009.1:n.5A>T
|
|
|
NM_024312.4:c.1346A>T
|
NP_077288.2:p.Asp449Val
|
|
XM_006719593.2:c.1346A>T
|
XP_006719656.1:p.Asp449Val
|
|
XM_011538731.1:c.1265A>T
|
XP_011537033.1:p.Asp422Val
|
|
XM_006719593.3:c.1346A>T
|
XP_006719656.1:p.Asp449Val
|
|
XM_011538731.2:c.1265A>T
|
XP_011537033.1:p.Asp422Val
|
|
XM_017019961.1:c.1130A>T
|
XP_016875450.1:p.Asp377Val
|
|
XM_017019962.2:c.119A>T
|
XP_016875451.1:p.Asp40Val
|
|
NM_024312.5:c.1346A>T
MANE Select
|
NP_077288.2:p.Asp449Val
|
|