ENST00000391944.8:c.872G>T
|
ENSP00000375808.4:p.Gly291Val
|
|
ENST00000682414.1:c.872G>T
|
ENSP00000507019.1:p.Gly291Val
|
|
ENST00000682508.1:n.901G>T
|
|
|
ENST00000684218.1:c.*130G>T
|
ENSP00000507804.1:n.*130G>T
|
|
ENST00000684407.1:c.749G>T
|
ENSP00000507775.1:p.Gly250Val
|
|
ENST00000684458.1:c.872G>T
|
ENSP00000508260.1:p.Gly291Val
|
|
ENST00000391945.10:c.872G>T
MANE Select
|
ENSP00000375809.4:p.Gly291Val
|
|
ENST00000586131.6:c.800G>T
|
ENSP00000464887.1:p.Gly267Val
|
|
ENST00000646507.1:n.969G>T
|
|
|
ENST00000391941.6:c.800G>T
|
ENSP00000375805.2:p.Gly267Val
|
|
ENST00000391944.7:c.638G>T
|
ENSP00000375808.3:p.Gly213Val
|
|
ENST00000391945.8:c.872G>T
|
ENSP00000375809.3:p.Gly291Val
|
|
ENST00000485403.6:c.800G>T
|
ENSP00000431229.2:p.Gly267Val
|
|
ENST00000586131.5:c.800G>T
|
ENSP00000464887.1:p.Gly267Val
|
|
ENST00000591309.5:c.*130G>T
|
ENSP00000465207.1:n.*130G>T
|
|
NM_000400.3:c.872G>T , LRG_461t1:c.872G>T
|
NP_000391.1:p.Gly291Val
|
|
NM_001130867.1:c.800G>T
|
NP_001124339.1:p.Gly267Val
|
|
XM_011526611.1:c.794G>T
|
XP_011524913.1:p.Gly265Val
|
|
XR_935763.1:n.919G>T
|
|
|
XM_011526611.2:c.794G>T
|
XP_011524913.1:p.Gly265Val
|
|
XM_017026467.1:c.749G>T
|
XP_016881956.1:p.Gly250Val
|
|
XR_001753633.2:n.919G>T
|
|
|
XR_001753634.2:n.919G>T
|
|
|
NM_000400.4:c.872G>T
MANE Select
|
NP_000391.1:p.Gly291Val
|
|
NM_001130867.2:c.800G>T
|
NP_001124339.1:p.Gly267Val
|
|