ENST00000682153.1:c.*225T>A
|
ENSP00000507923.1:n.*225T>A
|
|
ENST00000682358.1:n.11201T>A
|
|
|
ENST00000683334.1:c.*6813T>A
|
ENSP00000507369.1:n.*6813T>A
|
|
ENST00000357162.7:c.11056T>A
MANE Select
|
ENSP00000349685.2:p.Ser3686Thr
|
|
ENST00000358544.7:c.11131T>A
MANE Plus Clinical
|
ENSP00000351346.2:p.Ser3711Thr
|
|
ENST00000357162.6:c.11056T>A
|
ENSP00000349685.2:p.Ser3686Thr
|
|
ENST00000358544.6:c.11131T>A
|
ENSP00000351346.2:p.Ser3711Thr
|
|
NM_017890.4:c.11131T>A , LRG_351t1:c.11131T>A
|
NP_060360.3:p.Ser3711Thr
|
|
NM_152564.4:c.11056T>A , LRG_351t2:c.11056T>A
|
NP_689777.3:p.Ser3686Thr
|
|
XM_005250800.2:c.11131T>A
|
XP_005250857.1:p.Ser3711Thr
|
|
XM_005250801.3:c.11131T>A
|
XP_005250858.1:p.Ser3711Thr
|
|
XM_011516848.1:c.11128T>A
|
XP_011515150.1:p.Ser3710Thr
|
|
XM_011516849.1:c.11053T>A
|
XP_011515151.1:p.Ser3685Thr
|
|
XM_011516850.1:c.10753T>A
|
XP_011515152.1:p.Ser3585Thr
|
|
XM_011516851.1:c.8017T>A
|
XP_011515153.1:p.Ser2673Thr
|
|
XM_011516852.1:c.8017T>A
|
XP_011515154.1:p.Ser2673Thr
|
|
XM_011516854.1:c.6910T>A
|
XP_011515156.1:p.Ser2304Thr
|
|
XM_005250800.3:c.11131T>A
|
XP_005250857.1:p.Ser3711Thr
|
|
XM_005250801.5:c.11131T>A
|
XP_005250858.1:p.Ser3711Thr
|
|
XM_011516848.2:c.11128T>A
|
XP_011515150.1:p.Ser3710Thr
|
|
XM_011516849.2:c.11053T>A
|
XP_011515151.1:p.Ser3685Thr
|
|
XM_011516850.2:c.10753T>A
|
XP_011515152.1:p.Ser3585Thr
|
|
XM_011516851.2:c.8017T>A
|
XP_011515153.1:p.Ser2673Thr
|
|
XM_011516852.2:c.8017T>A
|
XP_011515154.1:p.Ser2673Thr
|
|
XM_011516854.2:c.6910T>A
|
XP_011515156.1:p.Ser2304Thr
|
|
XM_017013109.1:c.10936T>A
|
XP_016868598.1:p.Ser3646Thr
|
|
XM_017013111.1:c.8017T>A
|
XP_016868600.1:p.Ser2673Thr
|
|
XM_017013112.1:c.6688T>A
|
XP_016868601.1:p.Ser2230Thr
|
|
XM_024447074.1:c.9916T>A
|
XP_024302842.1:p.Ser3306Thr
|
|
NM_017890.5:c.11131T>A
MANE Plus Clinical
|
NP_060360.3:p.Ser3711Thr
|
|
NM_152564.5:c.11056T>A
MANE Select
|
NP_689777.3:p.Ser3686Thr
|
|