ENST00000299155.10:c.663G>A
MANE Select
|
ENSP00000299155.6:p.Trp221Ter
|
|
ENST00000299155.9:c.663G>A
|
ENSP00000299155.5:p.Trp221Ter
|
|
ENST00000541086.5:n.1409G>A
|
|
|
ENST00000558590.1:n.626G>A
|
|
|
ENST00000559442.1:n.434G>A
|
|
|
ENST00000559525.1:c.284G>A
|
|
|
ENST00000559789.1:c.126+484G>A
|
|
|
NM_030943.3:c.663G>A , LRG_642t1:c.663G>A
|
NP_112205.2:p.Trp221Ter
|
|
XM_011537202.1:c.501G>A
|
XP_011535504.1:p.Trp167Ter
|
|
XM_011537203.1:c.501G>A
|
XP_011535505.1:p.Trp167Ter
|
|
XM_011537202.3:c.501G>A
|
XP_011535504.1:p.Trp167Ter
|
|
XM_011537203.3:c.501G>A
|
XP_011535505.1:p.Trp167Ter
|
|
XM_024449714.1:c.759G>A
|
XP_024305482.1:p.Trp253Ter
|
|
NM_030943.4:c.663G>A
MANE Select
|
NP_112205.2:p.Trp221Ter
|
|