ENST00000350026.11:c.3858C>T
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ENSP00000055163.8:p.Ala1286=
|
|
ENST00000414678.8:c.3927C>T
|
ENSP00000412835.3:p.Ala1309=
|
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ENST00000637015.2:c.4146C>T
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ENSP00000489729.2:p.Ala1382=
|
|
ENST00000346085.10:c.3897C>T
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ENSP00000344546.5:p.Ala1299=
|
|
ENST00000350026.10:c.3609C>T
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ENSP00000055163.7:p.Ala1203=
|
|
ENST00000414678.7:c.2175C>T
|
ENSP00000412835.2:p.Ala725=
|
|
ENST00000635849.1:c.1338C>T
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ENSP00000490948.1:p.Ala446=
|
|
ENST00000635957.1:c.972C>T
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ENSP00000490385.1:p.Ala324=
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ENST00000636930.2:c.4017C>T
MANE Select
|
ENSP00000490491.2:p.Ala1339=
|
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ENST00000636940.1:n.2014C>T
|
|
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ENST00000637015.1:c.1385C>T
|
|
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ENST00000637568.1:c.1299C>T
|
|
|
ENST00000637741.1:n.683C>T
|
|
|
ENST00000637810.1:c.1359C>T
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ENSP00000489636.1:p.Ala453=
|
|
ENST00000637904.1:c.1518C>T
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ENSP00000490550.1:p.Ala506=
|
|
ENST00000647938.1:c.3648C>T
|
ENSP00000498155.1:p.Ala1216=
|
|
ENST00000346085.9:c.3648C>T
|
ENSP00000344546.4:p.Ala1216=
|
|
ENST00000350026.9:c.3609C>T
|
ENSP00000055163.7:p.Ala1203=
|
|
ENST00000414678.6:c.2175C>T
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ENSP00000412835.2:p.Ala725=
|
|
NM_017519.2:c.3609C>T
|
NP_059989.2:p.Ala1203=
|
|
NM_020732.3:c.3648C>T
|
NP_065783.3:p.Ala1216=
|
|
XM_005267069.3:c.3768C>T
|
XP_005267126.2:p.Ala1256=
|
|
XM_011535984.1:c.2847C>T
|
XP_011534286.1:p.Ala949=
|
|
XM_011535985.1:c.2667C>T
|
XP_011534287.1:p.Ala889=
|
|
XM_011535986.1:c.2427C>T
|
XP_011534288.1:p.Ala809=
|
|
XM_011535987.1:c.2046C>T
|
XP_011534289.1:p.Ala682=
|
|
XM_011535988.1:c.909C>T
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XP_011534290.1:p.Ala303=
|
|
NM_001346813.1:c.3768C>T
|
NP_001333742.1:p.Ala1256=
|
|
NM_001363725.1:c.1518C>T
|
NP_001350654.1:p.Ala506=
|
|
XM_011535984.2:c.3978C>T
|
XP_011534286.2:p.Ala1326=
|
|
XM_011535988.3:c.909C>T
|
XP_011534290.1:p.Ala303=
|
|
XM_017011103.2:c.3879C>T
|
XP_016866592.1:p.Ala1293=
|
|
XM_017011104.1:c.3849C>T
|
XP_016866593.1:p.Ala1283=
|
|
XM_017011105.2:c.3819C>T
|
XP_016866594.1:p.Ala1273=
|
|
XM_017011106.2:c.3690C>T
|
XP_016866595.1:p.Ala1230=
|
|
XM_017011107.2:c.3669C>T
|
XP_016866596.1:p.Ala1223=
|
|
XR_002956289.1:n.4061C>T
|
|
|
NM_001363725.2:c.1518C>T
|
NP_001350654.1:p.Ala506=
|
|
NM_001371656.1:c.3897C>T
|
NP_001358585.1:p.Ala1299=
|
|
NM_001374820.1:c.3897C>T
|
NP_001361749.1:p.Ala1299=
|
|
NM_001374828.1:c.4017C>T
MANE Select
|
NP_001361757.1:p.Ala1339=
|
|
NM_017519.3:c.3858C>T
|
NP_059989.3:p.Ala1286=
|
|