ENST00000295754.10:c.976G>T
MANE Select
|
ENSP00000295754.5:p.Ala326Ser
|
|
ENST00000672866.1:n.2572G>T
|
|
|
ENST00000295754.9:c.976G>T
|
ENSP00000295754.5:p.Ala326Ser
|
|
ENST00000359013.4:c.1051G>T
|
ENSP00000351905.4:p.Ala351Ser
|
|
NM_001024847.2:c.1051G>T , LRG_779t1:c.1051G>T
|
NP_001020018.1:p.Ala351Ser
|
|
NM_003242.5:c.976G>T
|
NP_003233.4:p.Ala326Ser
|
|
XM_011534043.1:c.1003G>T
|
XP_011532345.1:p.Ala335Ser
|
|
XM_011534044.1:c.928G>T
|
XP_011532346.1:p.Ala310Ser
|
|
XM_011534045.1:c.871G>T
|
XP_011532347.1:p.Ala291Ser
|
|
XM_011534043.2:c.1003G>T
|
XP_011532345.1:p.Ala335Ser
|
|
XM_011534045.3:c.871G>T
|
XP_011532347.1:p.Ala291Ser
|
|
XM_017007106.1:c.871G>T
|
XP_016862595.1:p.Ala291Ser
|
|
NM_003242.6:c.976G>T
MANE Select
|
NP_003233.4:p.Ala326Ser
|
|