ENST00000295754.10:c.970A>G
MANE Select
|
ENSP00000295754.5:p.Ile324Val
|
|
ENST00000672866.1:n.2566A>G
|
|
|
ENST00000295754.9:c.970A>G
|
ENSP00000295754.5:p.Ile324Val
|
|
ENST00000359013.4:c.1045A>G
|
ENSP00000351905.4:p.Ile349Val
|
|
NM_001024847.2:c.1045A>G , LRG_779t1:c.1045A>G
|
NP_001020018.1:p.Ile349Val
|
|
NM_003242.5:c.970A>G
|
NP_003233.4:p.Ile324Val
|
|
XM_011534043.1:c.997A>G
|
XP_011532345.1:p.Ile333Val
|
|
XM_011534044.1:c.922A>G
|
XP_011532346.1:p.Ile308Val
|
|
XM_011534045.1:c.865A>G
|
XP_011532347.1:p.Ile289Val
|
|
XM_011534043.2:c.997A>G
|
XP_011532345.1:p.Ile333Val
|
|
XM_011534045.3:c.865A>G
|
XP_011532347.1:p.Ile289Val
|
|
XM_017007106.1:c.865A>G
|
XP_016862595.1:p.Ile289Val
|
|
NM_003242.6:c.970A>G
MANE Select
|
NP_003233.4:p.Ile324Val
|
|