ENST00000350026.11:c.4530A=
|
ENSP00000055163.8:p.Thr1510=
|
|
ENST00000414678.8:c.4599A=
|
ENSP00000412835.3:p.Thr1533=
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ENST00000637015.2:c.4818A=
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ENSP00000489729.2:p.Thr1606=
|
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ENST00000346085.10:c.4569A=
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ENSP00000344546.5:p.Thr1523=
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ENST00000350026.10:c.4281A=
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ENSP00000055163.7:p.Thr1427=
|
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ENST00000414678.7:c.2847A=
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ENSP00000412835.2:p.Thr949=
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ENST00000635849.1:c.2010A=
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ENSP00000490948.1:p.Thr670=
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ENST00000635957.1:c.1641A=
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ENSP00000490385.1:p.Thr547=
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ENST00000636227.1:n.3152A=
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ENST00000636254.1:n.609A=
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ENST00000636930.2:c.4689A=
MANE Select
|
ENSP00000490491.2:p.Thr1563=
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ENST00000636940.1:n.2686A=
|
|
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ENST00000637015.1:c.2057A=
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ENST00000637568.1:c.1971A=
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ENST00000637741.1:n.1355A=
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ENST00000637810.1:c.2031A=
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ENSP00000489636.1:p.Thr677=
|
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ENST00000637904.1:c.2190A=
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ENSP00000490550.1:p.Thr730=
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ENST00000647938.1:c.4320A=
|
ENSP00000498155.1:p.Thr1440=
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ENST00000346085.9:c.4320A=
|
ENSP00000344546.4:p.Thr1440=
|
|
ENST00000350026.9:c.4281A=
|
ENSP00000055163.7:p.Thr1427=
|
|
ENST00000414678.6:c.2847A=
|
ENSP00000412835.2:p.Thr949=
|
|
NM_017519.2:c.4281A=
|
NP_059989.2:p.Thr1427=
|
|
NM_020732.3:c.4320A=
|
NP_065783.3:p.Thr1440=
|
|
XM_005267069.3:c.4440A=
|
XP_005267126.2:p.Thr1480=
|
|
XM_011535984.1:c.3519A=
|
XP_011534286.1:p.Thr1173=
|
|
XM_011535985.1:c.3339A=
|
XP_011534287.1:p.Thr1113=
|
|
XM_011535986.1:c.3099A=
|
XP_011534288.1:p.Thr1033=
|
|
XM_011535987.1:c.2718A=
|
XP_011534289.1:p.Thr906=
|
|
XM_011535988.1:c.1581A=
|
XP_011534290.1:p.Thr527=
|
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NM_001346813.1:c.4440A=
|
NP_001333742.1:p.Thr1480=
|
|
NM_001363725.1:c.2190A=
|
NP_001350654.1:p.Thr730=
|
|
XM_011535984.2:c.4650A=
|
XP_011534286.2:p.Thr1550=
|
|
XM_011535988.3:c.1581A=
|
XP_011534290.1:p.Thr527=
|
|
XM_017011103.2:c.4551A=
|
XP_016866592.1:p.Thr1517=
|
|
XM_017011104.1:c.4521A=
|
XP_016866593.1:p.Thr1507=
|
|
XM_017011105.2:c.4491A=
|
XP_016866594.1:p.Thr1497=
|
|
XM_017011106.2:c.4362A=
|
XP_016866595.1:p.Thr1454=
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XM_017011107.2:c.4341A=
|
XP_016866596.1:p.Thr1447=
|
|
XR_002956289.1:n.4636A=
|
|
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NM_001363725.2:c.2190A=
|
NP_001350654.1:p.Thr730=
|
|
NM_001371656.1:c.4569A=
|
NP_001358585.1:p.Thr1523=
|
|
NM_001374820.1:c.4569A=
|
NP_001361749.1:p.Thr1523=
|
|
NM_001374828.1:c.4689A=
MANE Select
|
NP_001361757.1:p.Thr1563=
|
|
NM_017519.3:c.4530A=
|
NP_059989.3:p.Thr1510=
|
|