ENST00000350026.11:c.5016C>T
|
ENSP00000055163.8:p.Ile1672=
|
|
ENST00000414678.8:c.5085C>T
|
ENSP00000412835.3:p.Ile1695=
|
|
ENST00000637015.2:c.5304C>T
|
ENSP00000489729.2:p.Ile1768=
|
|
ENST00000346085.10:c.5055C>T
|
ENSP00000344546.5:p.Ile1685=
|
|
ENST00000350026.10:c.4767C>T
|
ENSP00000055163.7:p.Ile1589=
|
|
ENST00000414678.7:c.3333C>T
|
ENSP00000412835.2:p.Ile1111=
|
|
ENST00000635849.1:c.2496C>T
|
ENSP00000490948.1:p.Ile832=
|
|
ENST00000635957.1:c.2127C>T
|
ENSP00000490385.1:p.Ile709=
|
|
ENST00000636227.1:n.3638C>T
|
|
|
ENST00000636254.1:n.1095C>T
|
|
|
ENST00000636930.2:c.5175C>T
MANE Select
|
ENSP00000490491.2:p.Ile1725=
|
|
ENST00000636940.1:n.3172C>T
|
|
|
ENST00000637015.1:c.2543C>T
|
|
|
ENST00000637568.1:c.2457C>T
|
|
|
ENST00000637741.1:n.1841C>T
|
|
|
ENST00000637810.1:c.2517C>T
|
ENSP00000489636.1:p.Ile839=
|
|
ENST00000637904.1:c.2676C>T
|
ENSP00000490550.1:p.Ile892=
|
|
ENST00000647938.1:c.4806C>T
|
ENSP00000498155.1:p.Ile1602=
|
|
ENST00000346085.9:c.4806C>T
|
ENSP00000344546.4:p.Ile1602=
|
|
ENST00000350026.9:c.4767C>T
|
ENSP00000055163.7:p.Ile1589=
|
|
ENST00000414678.6:c.3333C>T
|
ENSP00000412835.2:p.Ile1111=
|
|
NM_017519.2:c.4767C>T
|
NP_059989.2:p.Ile1589=
|
|
NM_020732.3:c.4806C>T
|
NP_065783.3:p.Ile1602=
|
|
XM_005267069.3:c.4926C>T
|
XP_005267126.2:p.Ile1642=
|
|
XM_011535984.1:c.4005C>T
|
XP_011534286.1:p.Ile1335=
|
|
XM_011535985.1:c.3825C>T
|
XP_011534287.1:p.Ile1275=
|
|
XM_011535986.1:c.3585C>T
|
XP_011534288.1:p.Ile1195=
|
|
XM_011535987.1:c.3204C>T
|
XP_011534289.1:p.Ile1068=
|
|
XM_011535988.1:c.2067C>T
|
XP_011534290.1:p.Ile689=
|
|
NM_001346813.1:c.4926C>T
|
NP_001333742.1:p.Ile1642=
|
|
NM_001363725.1:c.2676C>T
|
NP_001350654.1:p.Ile892=
|
|
XM_011535984.2:c.5136C>T
|
XP_011534286.2:p.Ile1712=
|
|
XM_011535988.3:c.2067C>T
|
XP_011534290.1:p.Ile689=
|
|
XM_017011103.2:c.5037C>T
|
XP_016866592.1:p.Ile1679=
|
|
XM_017011104.1:c.5007C>T
|
XP_016866593.1:p.Ile1669=
|
|
XM_017011105.2:c.4977C>T
|
XP_016866594.1:p.Ile1659=
|
|
XM_017011106.2:c.4848C>T
|
XP_016866595.1:p.Ile1616=
|
|
XM_017011107.2:c.4827C>T
|
XP_016866596.1:p.Ile1609=
|
|
XR_002956289.1:n.5122C>T
|
|
|
NM_001363725.2:c.2676C>T
|
NP_001350654.1:p.Ile892=
|
|
NM_001371656.1:c.5055C>T
|
NP_001358585.1:p.Ile1685=
|
|
NM_001374820.1:c.5055C>T
|
NP_001361749.1:p.Ile1685=
|
|
NM_001374828.1:c.5175C>T
MANE Select
|
NP_001361757.1:p.Ile1725=
|
|
NM_017519.3:c.5016C>T
|
NP_059989.3:p.Ile1672=
|
|