ENST00000211998.10:c.1044G>T
MANE Select
|
ENSP00000211998.5:p.Val348=
|
|
ENST00000211998.8:c.1044G>T
|
ENSP00000211998.4:p.Val348=
|
|
ENST00000372755.7:c.1044G>T
|
ENSP00000361841.3:p.Val348=
|
|
ENST00000436396.1:c.60G>T
|
ENSP00000415489.1:p.Val20=
|
|
ENST00000478896.2:n.332-11837G>T
|
|
|
ENST00000623461.3:n.3847G>T
|
|
|
ENST00000624354.3:c.*799G>T
|
ENSP00000485551.1:n.*799G>T
|
|
NM_003373.3:c.1044G>T
|
NP_003364.1:p.Val348=
|
|
NM_014000.2:c.1044G>T , LRG_383t1:c.1044G>T
|
NP_054706.1:p.Val348=
|
|
XM_005270142.1:c.1047G>T
|
XP_005270199.1:p.Val349=
|
|
XM_005270143.1:c.1047G>T
|
XP_005270200.1:p.Val349=
|
|
XR_001747501.1:n.89+715C>A
|
|
|
NM_003373.4:c.1044G>T
|
NP_003364.1:p.Val348=
|
|
NM_014000.3:c.1044G>T
MANE Select
|
NP_054706.1:p.Val348=
|
|