ENST00000682028.1:c.1316G>T
|
ENSP00000507230.1:p.Gly439Val
|
|
ENST00000682268.1:n.1614G>T
|
|
|
ENST00000682676.1:n.717G>T
|
|
|
ENST00000682902.1:n.1618G>T
|
|
|
ENST00000683513.1:c.1316G>T
|
ENSP00000506809.1:p.Gly439Val
|
|
ENST00000263431.4:c.1316G>T
MANE Select
|
ENSP00000263431.3:p.Gly439Val
|
|
ENST00000263431.3:c.1316G>T
|
ENSP00000263431.3:p.Gly439Val
|
|
NM_001316329.1:c.1316G>T
|
NP_001303258.1:p.Gly439Val
|
|
NM_002739.3:c.1316G>T , LRG_669t1:c.1316G>T
|
NP_002730.1:p.Gly439Val
|
|
NM_002739.4:c.1316G>T
|
NP_002730.1:p.Gly439Val
|
|
XM_011527108.1:c.407G>T
|
XP_011525410.1:p.Gly136Val
|
|
NM_002739.5:c.1316G>T
MANE Select
|
NP_002730.1:p.Gly439Val
|
|
NM_001316329.2:c.1316G>T
|
NP_001303258.1:p.Gly439Val
|
|