ENST00000295754.10:c.782C>T
MANE Select
|
ENSP00000295754.5:p.Ala261Val
|
|
ENST00000672866.1:n.2378C>T
|
|
|
ENST00000295754.9:c.782C>T
|
ENSP00000295754.5:p.Ala261Val
|
|
ENST00000359013.4:c.857C>T
|
ENSP00000351905.4:p.Ala286Val
|
|
NM_001024847.2:c.857C>T , LRG_779t1:c.857C>T
|
NP_001020018.1:p.Ala286Val
|
|
NM_003242.5:c.782C>T
|
NP_003233.4:p.Ala261Val
|
|
XM_011534043.1:c.809C>T
|
XP_011532345.1:p.Ala270Val
|
|
XM_011534044.1:c.734C>T
|
XP_011532346.1:p.Ala245Val
|
|
XM_011534045.1:c.677C>T
|
XP_011532347.1:p.Ala226Val
|
|
XM_011534043.2:c.809C>T
|
XP_011532345.1:p.Ala270Val
|
|
XM_011534045.3:c.677C>T
|
XP_011532347.1:p.Ala226Val
|
|
XM_017007106.1:c.677C>T
|
XP_016862595.1:p.Ala226Val
|
|
NM_003242.6:c.782C>T
MANE Select
|
NP_003233.4:p.Ala261Val
|
|