ENST00000695853.1:c.6035A>T
|
ENSP00000512218.1:p.Glu2012Val
|
|
ENST00000423902.7:c.6035A>T
MANE Select
|
ENSP00000392028.1:p.Glu2012Val
|
|
ENST00000423902.6:c.6035A>T
|
ENSP00000392028.1:p.Glu2012Val
|
|
ENST00000524602.5:c.1717-9591A>T
|
ENSP00000437061.1:n.1717-9591A>T
|
|
ENST00000527921.1:n.526A>T
|
|
|
NM_001316690.1:c.1717-9591A>T
|
NP_001303619.1:n.1717-9591A>T
|
|
NM_017780.3:c.6035A>T
|
NP_060250.2:p.Glu2012Val
|
|
XM_011517553.1:c.6125A>T
|
XP_011515855.1:p.Glu2042Val
|
|
XM_011517554.1:c.6125A>T
|
XP_011515856.1:p.Glu2042Val
|
|
XM_011517555.1:c.6125A>T
|
XP_011515857.1:p.Glu2042Val
|
|
XM_011517556.1:c.6125A>T
|
XP_011515858.1:p.Glu2042Val
|
|
XM_011517557.1:c.4112A>T
|
XP_011515859.1:p.Glu1371Val
|
|
XM_011517558.1:c.3662A>T
|
XP_011515860.1:p.Glu1221Val
|
|
XM_011517559.1:c.2870A>T
|
XP_011515861.1:p.Glu957Val
|
|
XM_011517553.2:c.6125A>T
|
XP_011515855.1:p.Glu2042Val
|
|
XM_011517554.3:c.6125A>T
|
XP_011515856.1:p.Glu2042Val
|
|
XM_011517555.2:c.6125A>T
|
XP_011515857.1:p.Glu2042Val
|
|
XM_017013612.1:c.6125A>T
|
XP_016869101.1:p.Glu2042Val
|
|
XM_017013613.1:c.6035A>T
|
XP_016869102.1:p.Glu2012Val
|
|
NM_017780.4:c.6035A>T
MANE Select
|
NP_060250.2:p.Glu2012Val
|
|