ENST00000350026.11:c.4989C>A
|
ENSP00000055163.8:p.Thr1663=
|
|
ENST00000414678.8:c.5058C>A
|
ENSP00000412835.3:p.Thr1686=
|
|
ENST00000637015.2:c.5277C>A
|
ENSP00000489729.2:p.Thr1759=
|
|
ENST00000346085.10:c.5028C>A
|
ENSP00000344546.5:p.Thr1676=
|
|
ENST00000350026.10:c.4740C>A
|
ENSP00000055163.7:p.Thr1580=
|
|
ENST00000414678.7:c.3306C>A
|
ENSP00000412835.2:p.Thr1102=
|
|
ENST00000635849.1:c.2469C>A
|
ENSP00000490948.1:p.Thr823=
|
|
ENST00000635957.1:c.2100C>A
|
ENSP00000490385.1:p.Thr700=
|
|
ENST00000636227.1:n.3611C>A
|
|
|
ENST00000636254.1:n.1068C>A
|
|
|
ENST00000636930.2:c.5148C>A
MANE Select
|
ENSP00000490491.2:p.Thr1716=
|
|
ENST00000636940.1:n.3145C>A
|
|
|
ENST00000637015.1:c.2516C>A
|
|
|
ENST00000637568.1:c.2430C>A
|
|
|
ENST00000637741.1:n.1814C>A
|
|
|
ENST00000637810.1:c.2490C>A
|
ENSP00000489636.1:p.Thr830=
|
|
ENST00000637904.1:c.2649C>A
|
ENSP00000490550.1:p.Thr883=
|
|
ENST00000647938.1:c.4779C>A
|
ENSP00000498155.1:p.Thr1593=
|
|
ENST00000346085.9:c.4779C>A
|
ENSP00000344546.4:p.Thr1593=
|
|
ENST00000350026.9:c.4740C>A
|
ENSP00000055163.7:p.Thr1580=
|
|
ENST00000414678.6:c.3306C>A
|
ENSP00000412835.2:p.Thr1102=
|
|
NM_017519.2:c.4740C>A
|
NP_059989.2:p.Thr1580=
|
|
NM_020732.3:c.4779C>A
|
NP_065783.3:p.Thr1593=
|
|
XM_005267069.3:c.4899C>A
|
XP_005267126.2:p.Thr1633=
|
|
XM_011535984.1:c.3978C>A
|
XP_011534286.1:p.Thr1326=
|
|
XM_011535985.1:c.3798C>A
|
XP_011534287.1:p.Thr1266=
|
|
XM_011535986.1:c.3558C>A
|
XP_011534288.1:p.Thr1186=
|
|
XM_011535987.1:c.3177C>A
|
XP_011534289.1:p.Thr1059=
|
|
XM_011535988.1:c.2040C>A
|
XP_011534290.1:p.Thr680=
|
|
NM_001346813.1:c.4899C>A
|
NP_001333742.1:p.Thr1633=
|
|
NM_001363725.1:c.2649C>A
|
NP_001350654.1:p.Thr883=
|
|
XM_011535984.2:c.5109C>A
|
XP_011534286.2:p.Thr1703=
|
|
XM_011535988.3:c.2040C>A
|
XP_011534290.1:p.Thr680=
|
|
XM_017011103.2:c.5010C>A
|
XP_016866592.1:p.Thr1670=
|
|
XM_017011104.1:c.4980C>A
|
XP_016866593.1:p.Thr1660=
|
|
XM_017011105.2:c.4950C>A
|
XP_016866594.1:p.Thr1650=
|
|
XM_017011106.2:c.4821C>A
|
XP_016866595.1:p.Thr1607=
|
|
XM_017011107.2:c.4800C>A
|
XP_016866596.1:p.Thr1600=
|
|
XR_002956289.1:n.5095C>A
|
|
|
NM_001363725.2:c.2649C>A
|
NP_001350654.1:p.Thr883=
|
|
NM_001371656.1:c.5028C>A
|
NP_001358585.1:p.Thr1676=
|
|
NM_001374820.1:c.5028C>A
|
NP_001361749.1:p.Thr1676=
|
|
NM_001374828.1:c.5148C>A
MANE Select
|
NP_001361757.1:p.Thr1716=
|
|
NM_017519.3:c.4989C>A
|
NP_059989.3:p.Thr1663=
|
|