ENST00000350026.11:c.3864C=
|
ENSP00000055163.8:p.Thr1288=
|
|
ENST00000414678.8:c.3933C=
|
ENSP00000412835.3:p.Thr1311=
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ENST00000637015.2:c.4152C=
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ENSP00000489729.2:p.Thr1384=
|
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ENST00000346085.10:c.3903C=
|
ENSP00000344546.5:p.Thr1301=
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ENST00000350026.10:c.3615C=
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ENSP00000055163.7:p.Thr1205=
|
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ENST00000414678.7:c.2181C=
|
ENSP00000412835.2:p.Thr727=
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ENST00000635849.1:c.1344C=
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ENSP00000490948.1:p.Thr448=
|
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ENST00000635957.1:c.978C=
|
ENSP00000490385.1:p.Thr326=
|
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ENST00000636930.2:c.4023C=
MANE Select
|
ENSP00000490491.2:p.Thr1341=
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ENST00000636940.1:n.2020C=
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ENST00000637015.1:c.1391C=
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ENST00000637568.1:c.1305C=
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ENST00000637741.1:n.689C=
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ENST00000637810.1:c.1365C=
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ENSP00000489636.1:p.Thr455=
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ENST00000637904.1:c.1524C=
|
ENSP00000490550.1:p.Thr508=
|
|
ENST00000647938.1:c.3654C=
|
ENSP00000498155.1:p.Thr1218=
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ENST00000346085.9:c.3654C=
|
ENSP00000344546.4:p.Thr1218=
|
|
ENST00000350026.9:c.3615C=
|
ENSP00000055163.7:p.Thr1205=
|
|
ENST00000414678.6:c.2181C=
|
ENSP00000412835.2:p.Thr727=
|
|
NM_017519.2:c.3615C=
|
NP_059989.2:p.Thr1205=
|
|
NM_020732.3:c.3654C=
|
NP_065783.3:p.Thr1218=
|
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XM_005267069.3:c.3774C=
|
XP_005267126.2:p.Thr1258=
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|
XM_011535984.1:c.2853C=
|
XP_011534286.1:p.Thr951=
|
|
XM_011535985.1:c.2673C=
|
XP_011534287.1:p.Thr891=
|
|
XM_011535986.1:c.2433C=
|
XP_011534288.1:p.Thr811=
|
|
XM_011535987.1:c.2052C=
|
XP_011534289.1:p.Thr684=
|
|
XM_011535988.1:c.915C=
|
XP_011534290.1:p.Thr305=
|
|
NM_001346813.1:c.3774C=
|
NP_001333742.1:p.Thr1258=
|
|
NM_001363725.1:c.1524C=
|
NP_001350654.1:p.Thr508=
|
|
XM_011535984.2:c.3984C=
|
XP_011534286.2:p.Thr1328=
|
|
XM_011535988.3:c.915C=
|
XP_011534290.1:p.Thr305=
|
|
XM_017011103.2:c.3885C=
|
XP_016866592.1:p.Thr1295=
|
|
XM_017011104.1:c.3855C=
|
XP_016866593.1:p.Thr1285=
|
|
XM_017011105.2:c.3825C=
|
XP_016866594.1:p.Thr1275=
|
|
XM_017011106.2:c.3696C=
|
XP_016866595.1:p.Thr1232=
|
|
XM_017011107.2:c.3675C=
|
XP_016866596.1:p.Thr1225=
|
|
XR_002956289.1:n.4067C=
|
|
|
NM_001363725.2:c.1524C=
|
NP_001350654.1:p.Thr508=
|
|
NM_001371656.1:c.3903C=
|
NP_001358585.1:p.Thr1301=
|
|
NM_001374820.1:c.3903C=
|
NP_001361749.1:p.Thr1301=
|
|
NM_001374828.1:c.4023C=
MANE Select
|
NP_001361757.1:p.Thr1341=
|
|
NM_017519.3:c.3864C=
|
NP_059989.3:p.Thr1288=
|
|