ENST00000695850.1:n.926G>T
|
|
|
ENST00000695851.1:n.130G>T
|
|
|
ENST00000695853.1:c.*809G>T
|
ENSP00000512218.1:n.*809G>T
|
|
ENST00000423902.7:c.7750G>T
MANE Select
|
ENSP00000392028.1:p.Asp2584Tyr
|
|
ENST00000423902.6:c.7750G>T
|
ENSP00000392028.1:p.Asp2584Tyr
|
|
ENST00000524602.5:c.1717-1184G>T
|
ENSP00000437061.1:n.1717-1184G>T
|
|
ENST00000531695.1:n.174G>T
|
|
|
ENST00000618450.1:n.142G>T
|
|
|
NM_001316690.1:c.1717-1184G>T
|
NP_001303619.1:n.1717-1184G>T
|
|
NM_017780.3:c.7750G>T
|
NP_060250.2:p.Asp2584Tyr
|
|
XM_011517553.1:c.7840G>T
|
XP_011515855.1:p.Asp2614Tyr
|
|
XM_011517554.1:c.7840G>T
|
XP_011515856.1:p.Asp2614Tyr
|
|
XM_011517555.1:c.7837G>T
|
XP_011515857.1:p.Asp2613Tyr
|
|
XM_011517556.1:c.7699-1151G>T
|
XP_011515858.1:n.7699-1151G>T
|
|
XM_011517557.1:c.5827G>T
|
XP_011515859.1:p.Asp1943Tyr
|
|
XM_011517558.1:c.5377G>T
|
XP_011515860.1:p.Asp1793Tyr
|
|
XM_011517559.1:c.4585G>T
|
XP_011515861.1:p.Asp1529Tyr
|
|
XM_011517553.2:c.7840G>T
|
XP_011515855.1:p.Asp2614Tyr
|
|
XM_011517554.3:c.7840G>T
|
XP_011515856.1:p.Asp2614Tyr
|
|
XM_011517555.2:c.7837G>T
|
XP_011515857.1:p.Asp2613Tyr
|
|
XM_017013612.1:c.7840G>T
|
XP_016869101.1:p.Asp2614Tyr
|
|
XM_017013613.1:c.7747G>T
|
XP_016869102.1:p.Asp2583Tyr
|
|
NM_017780.4:c.7750G>T
MANE Select
|
NP_060250.2:p.Asp2584Tyr
|
|