|
ENST00000485729.2:c.797G>T
(HFE)
|
ENSP00000417534.2:p.Gly266Val
|
|
|
ENST00000707188.1:c.391-1831C>A
(H2BC4)
|
ENSP00000516775.1:n.391-1831C>A
|
|
|
ENST00000357618.10:c.797G>T
(HFE)
MANE Select
|
ENSP00000417404.1:p.Gly266Val
|
|
|
ENST00000309234.10:c.797G>T
(HFE)
|
ENSP00000311698.6:p.Gly266Val
|
|
|
ENST00000317896.11:c.521G>T
(HFE)
|
ENSP00000313776.7:p.Gly174Val
|
|
|
ENST00000336625.12:c.479G>T
(HFE)
|
ENSP00000337819.8:p.Gly160Val
|
|
|
ENST00000349999.8:c.533G>T
(HFE)
|
ENSP00000259699.6:p.Gly178Val
|
|
|
ENST00000352392.8:c.77-254G>T
(HFE)
|
ENSP00000315936.4:n.77-254G>T
|
|
|
ENST00000353147.9:c.257G>T
(HFE)
|
ENSP00000312342.5:p.Gly86Val
|
|
|
ENST00000357618.9:c.797G>T
(HFE)
|
ENSP00000417404.1:p.Gly266Val
|
|
|
ENST00000397022.7:c.728G>T
(HFE)
|
ENSP00000380217.3:p.Gly243Val
|
|
|
ENST00000461397.5:c.755G>T
(HFE)
|
ENSP00000420802.1:p.Gly252Val
|
|
|
ENST00000470149.5:c.788G>T
(HFE)
|
ENSP00000419725.1:p.Gly263Val
|
|
|
ENST00000483782.1:n.1128G>T
(HFE)
|
|
|
|
ENST00000486147.1:n.640G>T
(HFE)
|
|
|
|
ENST00000488199.5:c.491G>T
(HFE)
|
ENSP00000420559.1:p.Gly164Val
|
|
|
ENST00000629531.1:c.132+30908C>A
(H2BC3)
|
ENSP00000486472.1:n.132+30908C>A
|
|
|
NM_000410.3:c.797G>T , LRG_748t1:c.797G>T
(HFE)
|
NP_000401.1:p.Gly266Val
|
|
|
NM_001300749.1:c.797G>T
(HFE)
|
NP_001287678.1:p.Gly266Val
|
|
|
NM_139003.2:c.479G>T
(HFE)
|
NP_620572.1:p.Gly160Val
|
|
|
NM_139004.2:c.521G>T
(HFE)
|
NP_620573.1:p.Gly174Val
|
|
|
NM_139006.2:c.755G>T
(HFE)
|
NP_620575.1:p.Gly252Val
|
|
|
NM_139007.2:c.533G>T
(HFE)
|
NP_620576.1:p.Gly178Val
|
|
|
NM_139008.2:c.491G>T
(HFE)
|
NP_620577.1:p.Gly164Val
|
|
|
NM_139009.2:c.728G>T
(HFE)
|
NP_620578.1:p.Gly243Val
|
|
|
NM_139010.2:c.257G>T
(HFE)
|
NP_620579.1:p.Gly86Val
|
|
|
NM_139011.2:c.77-254G>T
(HFE)
|
NP_620580.1:n.77-254G>T
|
|
|
XM_011514543.1:c.797G>T
(HFE)
|
XP_011512845.1:p.Gly266Val
|
|
|
XM_011514544.1:c.788G>T
(HFE)
|
XP_011512846.1:p.Gly263Val
|
|
|
XR_241893.2:n.919G>T
(HFE)
|
|
|
|
XM_011514543.3:c.797G>T
(HFE)
|
XP_011512845.1:p.Gly266Val
|
|
|
XR_241893.4:n.891G>T
(HFE)
|
|
|
|
NM_001300749.2:c.797G>T
(HFE)
|
NP_001287678.1:p.Gly266Val
|
|
|
NM_139003.3:c.479G>T
(HFE)
|
NP_620572.1:p.Gly160Val
|
|
|
NM_139004.3:c.521G>T
(HFE)
|
NP_620573.1:p.Gly174Val
|
|
|
NM_139006.3:c.755G>T
(HFE)
|
NP_620575.1:p.Gly252Val
|
|
|
NM_139007.3:c.533G>T
(HFE)
|
NP_620576.1:p.Gly178Val
|
|
|
NM_139008.3:c.491G>T
(HFE)
|
NP_620577.1:p.Gly164Val
|
|
|
NM_139009.3:c.728G>T
(HFE)
|
NP_620578.1:p.Gly243Val
|
|
|
NM_139010.3:c.257G>T
(HFE)
|
NP_620579.1:p.Gly86Val
|
|
|
NM_139011.3:c.77-254G>T
(HFE)
|
NP_620580.1:n.77-254G>T
|
|
|
NM_000410.4:c.797G>T
(HFE)
MANE Select
|
NP_000401.1:p.Gly266Val
|
|
|
NM_001384164.1:c.797G>T
(HFE)
|
NP_001371093.1:p.Gly266Val
|
|
