ENST00000695850.1:n.912G>T
|
|
|
ENST00000695851.1:n.116G>T
|
|
|
ENST00000695853.1:c.*795G>T
|
ENSP00000512218.1:n.*795G>T
|
|
ENST00000423902.7:c.7736G>T
MANE Select
|
ENSP00000392028.1:p.Arg2579Met
|
|
ENST00000423902.6:c.7736G>T
|
ENSP00000392028.1:p.Arg2579Met
|
|
ENST00000524602.5:c.1717-1198G>T
|
ENSP00000437061.1:n.1717-1198G>T
|
|
ENST00000531695.1:n.160G>T
|
|
|
ENST00000618450.1:n.128G>T
|
|
|
NM_001316690.1:c.1717-1198G>T
|
NP_001303619.1:n.1717-1198G>T
|
|
NM_017780.3:c.7736G>T
|
NP_060250.2:p.Arg2579Met
|
|
XM_011517553.1:c.7826G>T
|
XP_011515855.1:p.Arg2609Met
|
|
XM_011517554.1:c.7826G>T
|
XP_011515856.1:p.Arg2609Met
|
|
XM_011517555.1:c.7823G>T
|
XP_011515857.1:p.Arg2608Met
|
|
XM_011517556.1:c.7699-1165G>T
|
XP_011515858.1:n.7699-1165G>T
|
|
XM_011517557.1:c.5813G>T
|
XP_011515859.1:p.Arg1938Met
|
|
XM_011517558.1:c.5363G>T
|
XP_011515860.1:p.Arg1788Met
|
|
XM_011517559.1:c.4571G>T
|
XP_011515861.1:p.Arg1524Met
|
|
XM_011517553.2:c.7826G>T
|
XP_011515855.1:p.Arg2609Met
|
|
XM_011517554.3:c.7826G>T
|
XP_011515856.1:p.Arg2609Met
|
|
XM_011517555.2:c.7823G>T
|
XP_011515857.1:p.Arg2608Met
|
|
XM_017013612.1:c.7826G>T
|
XP_016869101.1:p.Arg2609Met
|
|
XM_017013613.1:c.7733G>T
|
XP_016869102.1:p.Arg2578Met
|
|
NM_017780.4:c.7736G>T
MANE Select
|
NP_060250.2:p.Arg2579Met
|
|