ENST00000682153.1:c.7353T>C
|
ENSP00000507923.1:p.Thr2451=
|
|
ENST00000682358.1:n.7423T>C
|
|
|
ENST00000683334.1:c.*3035T>C
|
ENSP00000507369.1:n.*3035T>C
|
|
ENST00000357162.7:c.7278T>C
MANE Select
|
ENSP00000349685.2:p.Thr2426=
|
|
ENST00000358544.7:c.7353T>C
MANE Plus Clinical
|
ENSP00000351346.2:p.Thr2451=
|
|
ENST00000357162.6:c.7278T>C
|
ENSP00000349685.2:p.Thr2426=
|
|
ENST00000358544.6:c.7353T>C
|
ENSP00000351346.2:p.Thr2451=
|
|
ENST00000518569.1:n.378-1877T>C
|
|
|
NM_017890.4:c.7353T>C , LRG_351t1:c.7353T>C
|
NP_060360.3:p.Thr2451=
|
|
NM_152564.4:c.7278T>C , LRG_351t2:c.7278T>C
|
NP_689777.3:p.Thr2426=
|
|
XM_005250800.2:c.7353T>C
|
XP_005250857.1:p.Thr2451=
|
|
XM_005250801.3:c.7353T>C
|
XP_005250858.1:p.Thr2451=
|
|
XM_011516848.1:c.7350T>C
|
XP_011515150.1:p.Thr2450=
|
|
XM_011516849.1:c.7275T>C
|
XP_011515151.1:p.Thr2425=
|
|
XM_011516850.1:c.6975T>C
|
XP_011515152.1:p.Thr2325=
|
|
XM_011516851.1:c.4239T>C
|
XP_011515153.1:p.Thr1413=
|
|
XM_011516852.1:c.4239T>C
|
XP_011515154.1:p.Thr1413=
|
|
XM_011516853.1:c.7353T>C
|
XP_011515155.1:p.Thr2451=
|
|
XM_011516854.1:c.3132T>C
|
XP_011515156.1:p.Thr1044=
|
|
XR_928446.1:n.1830+5673A>G
|
|
|
XM_005250800.3:c.7353T>C
|
XP_005250857.1:p.Thr2451=
|
|
XM_005250801.5:c.7353T>C
|
XP_005250858.1:p.Thr2451=
|
|
XM_011516848.2:c.7350T>C
|
XP_011515150.1:p.Thr2450=
|
|
XM_011516849.2:c.7275T>C
|
XP_011515151.1:p.Thr2425=
|
|
XM_011516850.2:c.6975T>C
|
XP_011515152.1:p.Thr2325=
|
|
XM_011516851.2:c.4239T>C
|
XP_011515153.1:p.Thr1413=
|
|
XM_011516852.2:c.4239T>C
|
XP_011515154.1:p.Thr1413=
|
|
XM_011516853.2:c.7353T>C
|
XP_011515155.1:p.Thr2451=
|
|
XM_011516854.2:c.3132T>C
|
XP_011515156.1:p.Thr1044=
|
|
XM_017013109.1:c.7158T>C
|
XP_016868598.1:p.Thr2386=
|
|
XM_017013111.1:c.4239T>C
|
XP_016868600.1:p.Thr1413=
|
|
XM_017013112.1:c.2910T>C
|
XP_016868601.1:p.Thr970=
|
|
XM_024447074.1:c.6138T>C
|
XP_024302842.1:p.Thr2046=
|
|
NM_017890.5:c.7353T>C
MANE Plus Clinical
|
NP_060360.3:p.Thr2451=
|
|
NM_152564.5:c.7278T>C
MANE Select
|
NP_689777.3:p.Thr2426=
|
|