|
ENST00000400345.8:c.79G=
MANE Select
|
ENSP00000383199.2:p.Val27=
|
|
|
ENST00000585594.6:n.56G=
|
|
|
|
ENST00000674613.1:n.98-79609G=
|
|
|
|
ENST00000674845.1:c.*585G=
|
ENSP00000502309.1:n.*585G=
|
|
|
ENST00000675137.1:n.201G=
|
|
|
|
ENST00000675147.1:c.58G=
|
ENSP00000501840.1:p.Val20=
|
|
|
ENST00000675502.1:c.-285G=
|
ENSP00000502428.1:n.-285G=
|
|
|
ENST00000675801.1:c.-285G=
|
ENSP00000502688.1:n.-285G=
|
|
|
ENST00000676024.1:c.79G=
|
ENSP00000502105.1:p.Val27=
|
|
|
ENST00000676223.1:c.40G=
|
ENSP00000502361.1:p.Val14=
|
|
|
ENST00000256830.13:c.79G=
|
ENSP00000256830.8:p.Val27=
|
|
|
ENST00000356462.10:c.79G=
|
ENSP00000348847.5:p.Val27=
|
|
|
ENST00000357895.9:c.55G=
|
ENSP00000350569.4:p.Val19=
|
|
|
ENST00000382850.8:c.79G=
|
ENSP00000372301.3:p.Val27=
|
|
|
ENST00000400345.7:c.79G=
|
ENSP00000383199.2:p.Val27=
|
|
|
ENST00000435432.6:c.-363G=
|
ENSP00000393395.1:n.-363G=
|
|
|
ENST00000456986.5:c.-285G=
|
ENSP00000411947.1:n.-285G=
|
|
|
ENST00000585363.5:n.116G=
|
|
|
|
ENST00000585594.5:n.199G=
|
|
|
|
ENST00000586263.5:c.55G=
|
ENSP00000468546.1:p.Val19=
|
|
|
ENST00000587547.1:n.868G=
|
|
|
|
ENST00000588516.5:n.1179G=
|
|
|
|
ENST00000589054.5:c.48+121110G=
|
ENSP00000465669.1:n.48+121110G=
|
|
|
ENST00000590694.5:n.122G=
|
|
|
|
ENST00000591579.5:n.123G=
|
|
|
|
ENST00000591989.5:n.127G=
|
|
|
|
ENST00000592846.5:c.-344G=
|
ENSP00000466776.1:n.-344G=
|
|
|
NM_001144964.1:c.-285G=
|
NP_001138436.1:n.-285G=
|
|
|
NM_001144965.1:c.-285G=
|
NP_001138437.1:n.-285G=
|
|
|
NM_001144967.2:c.79G=
|
NP_001138439.1:p.Val27=
|
|
|
NM_001144968.1:c.55G=
|
NP_001138440.1:p.Val19=
|
|
|
NM_001144969.1:c.55G=
|
NP_001138441.1:p.Val19=
|
|
|
NM_001144971.1:c.-363G=
|
NP_001138443.1:n.-363G=
|
|
|
NM_001243960.1:c.79G=
|
NP_001230889.1:p.Val27=
|
|
|
NM_015277.5:c.79G=
|
NP_056092.2:p.Val27=
|
|
|
XM_006722426.2:c.79G=
|
XP_006722489.1:p.Val27=
|
|
|
XM_006722428.2:c.79G=
|
XP_006722491.1:p.Val27=
|
|
|
XM_011525887.1:c.55G=
|
XP_011524189.1:p.Val19=
|
|
|
XM_006722426.4:c.79G=
|
XP_006722489.1:p.Val27=
|
|
|
XM_006722428.4:c.79G=
|
XP_006722491.1:p.Val27=
|
|
|
XM_011525887.3:c.55G=
|
XP_011524189.1:p.Val19=
|
|
|
XM_017025678.2:c.79G=
|
XP_016881167.1:p.Val27=
|
|
|
XM_024451129.1:c.-363G=
|
XP_024306897.1:n.-363G=
|
|
|
XM_024451131.1:c.-285G=
|
XP_024306899.1:n.-285G=
|
|
|
XM_024451134.1:c.-344G=
|
XP_024306902.1:n.-344G=
|
|
|
XM_024451135.1:c.-285G=
|
XP_024306903.1:n.-285G=
|
|
|
XM_024451136.1:c.-285G=
|
XP_024306904.1:n.-285G=
|
|
|
XM_024451137.1:c.-363G=
|
XP_024306905.1:n.-363G=
|
|
|
NM_001144967.3:c.79G=
MANE Select
|
NP_001138439.1:p.Val27=
|
|
|
NM_001144965.2:c.-285G=
|
NP_001138437.1:n.-285G=
|
|
|
NM_001144968.2:c.55G=
|
NP_001138440.1:p.Val19=
|
|
|
NM_001144969.2:c.55G=
|
NP_001138441.1:p.Val19=
|
|
|
NM_001144971.2:c.-363G=
|
NP_001138443.1:n.-363G=
|
|
|
NM_001243960.2:c.79G=
|
NP_001230889.1:p.Val27=
|
|
|
NM_015277.6:c.79G=
|
NP_056092.2:p.Val27=
|
|
