ENST00000695850.1:n.812G>T
|
|
|
ENST00000695851.1:n.16G>T
|
|
|
ENST00000695853.1:c.*695G>T
|
ENSP00000512218.1:n.*695G>T
|
|
ENST00000423902.7:c.7636G>T
MANE Select
|
ENSP00000392028.1:p.Glu2546Ter
|
|
ENST00000423902.6:c.7636G>T
|
ENSP00000392028.1:p.Glu2546Ter
|
|
ENST00000524602.5:c.1717-1298G>T
|
ENSP00000437061.1:n.1717-1298G>T
|
|
ENST00000531695.1:n.60G>T
|
|
|
ENST00000618450.1:n.28G>T
|
|
|
NM_001316690.1:c.1717-1298G>T
|
NP_001303619.1:n.1717-1298G>T
|
|
NM_017780.3:c.7636G>T
|
NP_060250.2:p.Glu2546Ter
|
|
XM_011517553.1:c.7726G>T
|
XP_011515855.1:p.Glu2576Ter
|
|
XM_011517554.1:c.7726G>T
|
XP_011515856.1:p.Glu2576Ter
|
|
XM_011517555.1:c.7723G>T
|
XP_011515857.1:p.Glu2575Ter
|
|
XM_011517556.1:c.7699-1265G>T
|
XP_011515858.1:n.7699-1265G>T
|
|
XM_011517557.1:c.5713G>T
|
XP_011515859.1:p.Glu1905Ter
|
|
XM_011517558.1:c.5263G>T
|
XP_011515860.1:p.Glu1755Ter
|
|
XM_011517559.1:c.4471G>T
|
XP_011515861.1:p.Glu1491Ter
|
|
XM_011517553.2:c.7726G>T
|
XP_011515855.1:p.Glu2576Ter
|
|
XM_011517554.3:c.7726G>T
|
XP_011515856.1:p.Glu2576Ter
|
|
XM_011517555.2:c.7723G>T
|
XP_011515857.1:p.Glu2575Ter
|
|
XM_017013612.1:c.7726G>T
|
XP_016869101.1:p.Glu2576Ter
|
|
XM_017013613.1:c.7633G>T
|
XP_016869102.1:p.Glu2545Ter
|
|
NM_017780.4:c.7636G>T
MANE Select
|
NP_060250.2:p.Glu2546Ter
|
|