ENST00000682153.1:c.*268G>A
|
ENSP00000507923.1:n.*268G>A
|
|
ENST00000682358.1:n.11244G>A
|
|
|
ENST00000683334.1:c.*6856G>A
|
ENSP00000507369.1:n.*6856G>A
|
|
ENST00000357162.7:c.11099G>A
MANE Select
|
ENSP00000349685.2:p.Arg3700Gln
|
|
ENST00000358544.7:c.11174G>A
MANE Plus Clinical
|
ENSP00000351346.2:p.Arg3725Gln
|
|
ENST00000357162.6:c.11099G>A
|
ENSP00000349685.2:p.Arg3700Gln
|
|
ENST00000358544.6:c.11174G>A
|
ENSP00000351346.2:p.Arg3725Gln
|
|
NM_017890.4:c.11174G>A , LRG_351t1:c.11174G>A
|
NP_060360.3:p.Arg3725Gln
|
|
NM_152564.4:c.11099G>A , LRG_351t2:c.11099G>A
|
NP_689777.3:p.Arg3700Gln
|
|
XM_005250800.2:c.11174G>A
|
XP_005250857.1:p.Arg3725Gln
|
|
XM_005250801.3:c.11174G>A
|
XP_005250858.1:p.Arg3725Gln
|
|
XM_011516848.1:c.11171G>A
|
XP_011515150.1:p.Arg3724Gln
|
|
XM_011516849.1:c.11096G>A
|
XP_011515151.1:p.Arg3699Gln
|
|
XM_011516850.1:c.10796G>A
|
XP_011515152.1:p.Arg3599Gln
|
|
XM_011516851.1:c.8060G>A
|
XP_011515153.1:p.Arg2687Gln
|
|
XM_011516852.1:c.8060G>A
|
XP_011515154.1:p.Arg2687Gln
|
|
XM_011516854.1:c.6953G>A
|
XP_011515156.1:p.Arg2318Gln
|
|
XM_005250800.3:c.11174G>A
|
XP_005250857.1:p.Arg3725Gln
|
|
XM_005250801.5:c.11174G>A
|
XP_005250858.1:p.Arg3725Gln
|
|
XM_011516848.2:c.11171G>A
|
XP_011515150.1:p.Arg3724Gln
|
|
XM_011516849.2:c.11096G>A
|
XP_011515151.1:p.Arg3699Gln
|
|
XM_011516850.2:c.10796G>A
|
XP_011515152.1:p.Arg3599Gln
|
|
XM_011516851.2:c.8060G>A
|
XP_011515153.1:p.Arg2687Gln
|
|
XM_011516852.2:c.8060G>A
|
XP_011515154.1:p.Arg2687Gln
|
|
XM_011516854.2:c.6953G>A
|
XP_011515156.1:p.Arg2318Gln
|
|
XM_017013109.1:c.10979G>A
|
XP_016868598.1:p.Arg3660Gln
|
|
XM_017013111.1:c.8060G>A
|
XP_016868600.1:p.Arg2687Gln
|
|
XM_017013112.1:c.6731G>A
|
XP_016868601.1:p.Arg2244Gln
|
|
XM_024447074.1:c.9959G>A
|
XP_024302842.1:p.Arg3320Gln
|
|
NM_017890.5:c.11174G>A
MANE Plus Clinical
|
NP_060360.3:p.Arg3725Gln
|
|
NM_152564.5:c.11099G>A
MANE Select
|
NP_689777.3:p.Arg3700Gln
|
|