ENST00000682153.1:c.*349G>T
|
ENSP00000507923.1:n.*349G>T
|
|
ENST00000682358.1:n.11325G>T
|
|
|
ENST00000683334.1:c.*6937G>T
|
ENSP00000507369.1:n.*6937G>T
|
|
ENST00000357162.7:c.11180G>T
MANE Select
|
ENSP00000349685.2:p.Arg3727Leu
|
|
ENST00000358544.7:c.11255G>T
MANE Plus Clinical
|
ENSP00000351346.2:p.Arg3752Leu
|
|
ENST00000357162.6:c.11180G>T
|
ENSP00000349685.2:p.Arg3727Leu
|
|
ENST00000358544.6:c.11255G>T
|
ENSP00000351346.2:p.Arg3752Leu
|
|
NM_017890.4:c.11255G>T , LRG_351t1:c.11255G>T
|
NP_060360.3:p.Arg3752Leu
|
|
NM_152564.4:c.11180G>T , LRG_351t2:c.11180G>T
|
NP_689777.3:p.Arg3727Leu
|
|
XM_005250800.2:c.11255G>T
|
XP_005250857.1:p.Arg3752Leu
|
|
XM_005250801.3:c.11255G>T
|
XP_005250858.1:p.Arg3752Leu
|
|
XM_011516848.1:c.11252G>T
|
XP_011515150.1:p.Arg3751Leu
|
|
XM_011516849.1:c.11177G>T
|
XP_011515151.1:p.Arg3726Leu
|
|
XM_011516850.1:c.10877G>T
|
XP_011515152.1:p.Arg3626Leu
|
|
XM_011516851.1:c.8141G>T
|
XP_011515153.1:p.Arg2714Leu
|
|
XM_011516852.1:c.8141G>T
|
XP_011515154.1:p.Arg2714Leu
|
|
XM_011516854.1:c.7034G>T
|
XP_011515156.1:p.Arg2345Leu
|
|
XM_005250800.3:c.11255G>T
|
XP_005250857.1:p.Arg3752Leu
|
|
XM_005250801.5:c.11255G>T
|
XP_005250858.1:p.Arg3752Leu
|
|
XM_011516848.2:c.11252G>T
|
XP_011515150.1:p.Arg3751Leu
|
|
XM_011516849.2:c.11177G>T
|
XP_011515151.1:p.Arg3726Leu
|
|
XM_011516850.2:c.10877G>T
|
XP_011515152.1:p.Arg3626Leu
|
|
XM_011516851.2:c.8141G>T
|
XP_011515153.1:p.Arg2714Leu
|
|
XM_011516852.2:c.8141G>T
|
XP_011515154.1:p.Arg2714Leu
|
|
XM_011516854.2:c.7034G>T
|
XP_011515156.1:p.Arg2345Leu
|
|
XM_017013109.1:c.11060G>T
|
XP_016868598.1:p.Arg3687Leu
|
|
XM_017013111.1:c.8141G>T
|
XP_016868600.1:p.Arg2714Leu
|
|
XM_017013112.1:c.6812G>T
|
XP_016868601.1:p.Arg2271Leu
|
|
XM_024447074.1:c.10040G>T
|
XP_024302842.1:p.Arg3347Leu
|
|
NM_017890.5:c.11255G>T
MANE Plus Clinical
|
NP_060360.3:p.Arg3752Leu
|
|
NM_152564.5:c.11180G>T
MANE Select
|
NP_689777.3:p.Arg3727Leu
|
|