ENST00000695850.1:n.825A>T
|
|
|
ENST00000695851.1:n.29A>T
|
|
|
ENST00000695853.1:c.*708A>T
|
ENSP00000512218.1:n.*708A>T
|
|
ENST00000423902.7:c.7649A>T
MANE Select
|
ENSP00000392028.1:p.Glu2550Val
|
|
ENST00000423902.6:c.7649A>T
|
ENSP00000392028.1:p.Glu2550Val
|
|
ENST00000524602.5:c.1717-1285A>T
|
ENSP00000437061.1:n.1717-1285A>T
|
|
ENST00000531695.1:n.73A>T
|
|
|
ENST00000618450.1:n.41A>T
|
|
|
NM_001316690.1:c.1717-1285A>T
|
NP_001303619.1:n.1717-1285A>T
|
|
NM_017780.3:c.7649A>T
|
NP_060250.2:p.Glu2550Val
|
|
XM_011517553.1:c.7739A>T
|
XP_011515855.1:p.Glu2580Val
|
|
XM_011517554.1:c.7739A>T
|
XP_011515856.1:p.Glu2580Val
|
|
XM_011517555.1:c.7736A>T
|
XP_011515857.1:p.Glu2579Val
|
|
XM_011517556.1:c.7699-1252A>T
|
XP_011515858.1:n.7699-1252A>T
|
|
XM_011517557.1:c.5726A>T
|
XP_011515859.1:p.Glu1909Val
|
|
XM_011517558.1:c.5276A>T
|
XP_011515860.1:p.Glu1759Val
|
|
XM_011517559.1:c.4484A>T
|
XP_011515861.1:p.Glu1495Val
|
|
XM_011517553.2:c.7739A>T
|
XP_011515855.1:p.Glu2580Val
|
|
XM_011517554.3:c.7739A>T
|
XP_011515856.1:p.Glu2580Val
|
|
XM_011517555.2:c.7736A>T
|
XP_011515857.1:p.Glu2579Val
|
|
XM_017013612.1:c.7739A>T
|
XP_016869101.1:p.Glu2580Val
|
|
XM_017013613.1:c.7646A>T
|
XP_016869102.1:p.Glu2549Val
|
|
NM_017780.4:c.7649A>T
MANE Select
|
NP_060250.2:p.Glu2550Val
|
|