ENST00000397423.7:n.484+373G>T
|
|
|
ENST00000483204.2:n.879G>T
|
|
|
ENST00000495262.7:c.303G>T
MANE Select
|
ENSP00000419411.2:p.Val101=
|
|
ENST00000379597.7:c.303G>T
|
ENSP00000368917.3:p.Val101=
|
|
ENST00000397423.6:n.484+373G>T
|
|
|
ENST00000410107.5:c.67+20056G>T
|
ENSP00000386321.1:n.67+20056G>T
|
|
ENST00000474518.1:n.508+373G>T
|
|
|
ENST00000474983.5:n.880G>T
|
|
|
ENST00000475577.5:n.254+1554G>T
|
|
|
ENST00000483204.1:n.879G>T
|
|
|
ENST00000489225.5:n.283+36283G>T
|
|
|
ENST00000489819.5:n.175+7620G>T
|
|
|
ENST00000495262.5:c.303G>T
|
ENSP00000419411.1:p.Val101=
|
|
NM_145649.4:c.303G>T
|
NP_663624.1:p.Val101=
|
|
XM_005248999.2:c.72G>T
|
XP_005249056.1:p.Val24=
|
|
XM_006715052.2:c.303G>T
|
XP_006715115.1:p.Val101=
|
|
XM_006715053.2:c.303G>T
|
XP_006715116.1:p.Val101=
|
|
XM_011514465.1:c.303G>T
|
XP_011512767.1:p.Val101=
|
|
XM_011514467.1:c.72G>T
|
XP_011512769.1:p.Val24=
|
|
XM_011514468.1:c.303G>T
|
XP_011512770.1:p.Val101=
|
|
XR_926136.1:n.854G>T
|
|
|
XM_006715052.3:c.303G>T
|
XP_006715115.1:p.Val101=
|
|
XM_011514468.3:c.303G>T
|
XP_011512770.1:p.Val101=
|
|
XM_017010732.2:c.303G>T
|
XP_016866221.1:p.Val101=
|
|
XR_002956275.1:n.854G>T
|
|
|
XR_926136.2:n.852G>T
|
|
|
NM_001374747.1:c.303G>T
|
NP_001361676.1:p.Val101=
|
|
NM_145649.5:c.303G>T
MANE Select
|
NP_663624.1:p.Val101=
|
|