ENST00000695850.1:n.840G>T
|
|
|
ENST00000695851.1:n.44G>T
|
|
|
ENST00000695853.1:c.*723G>T
|
ENSP00000512218.1:n.*723G>T
|
|
ENST00000423902.7:c.7664G>T
MANE Select
|
ENSP00000392028.1:p.Arg2555Ile
|
|
ENST00000423902.6:c.7664G>T
|
ENSP00000392028.1:p.Arg2555Ile
|
|
ENST00000524602.5:c.1717-1270G>T
|
ENSP00000437061.1:n.1717-1270G>T
|
|
ENST00000531695.1:n.88G>T
|
|
|
ENST00000618450.1:n.56G>T
|
|
|
NM_001316690.1:c.1717-1270G>T
|
NP_001303619.1:n.1717-1270G>T
|
|
NM_017780.3:c.7664G>T
|
NP_060250.2:p.Arg2555Ile
|
|
XM_011517553.1:c.7754G>T
|
XP_011515855.1:p.Arg2585Ile
|
|
XM_011517554.1:c.7754G>T
|
XP_011515856.1:p.Arg2585Ile
|
|
XM_011517555.1:c.7751G>T
|
XP_011515857.1:p.Arg2584Ile
|
|
XM_011517556.1:c.7699-1237G>T
|
XP_011515858.1:n.7699-1237G>T
|
|
XM_011517557.1:c.5741G>T
|
XP_011515859.1:p.Arg1914Ile
|
|
XM_011517558.1:c.5291G>T
|
XP_011515860.1:p.Arg1764Ile
|
|
XM_011517559.1:c.4499G>T
|
XP_011515861.1:p.Arg1500Ile
|
|
XM_011517553.2:c.7754G>T
|
XP_011515855.1:p.Arg2585Ile
|
|
XM_011517554.3:c.7754G>T
|
XP_011515856.1:p.Arg2585Ile
|
|
XM_011517555.2:c.7751G>T
|
XP_011515857.1:p.Arg2584Ile
|
|
XM_017013612.1:c.7754G>T
|
XP_016869101.1:p.Arg2585Ile
|
|
XM_017013613.1:c.7661G>T
|
XP_016869102.1:p.Arg2554Ile
|
|
NM_017780.4:c.7664G>T
MANE Select
|
NP_060250.2:p.Arg2555Ile
|
|