ENST00000350026.11:c.4727T=
|
ENSP00000055163.8:p.Ile1576=
|
|
ENST00000414678.8:c.4796T=
|
ENSP00000412835.3:p.Ile1599=
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ENST00000637015.2:c.5015T=
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ENSP00000489729.2:p.Ile1672=
|
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ENST00000346085.10:c.4766T=
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ENSP00000344546.5:p.Ile1589=
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ENST00000350026.10:c.4478T=
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ENSP00000055163.7:p.Ile1493=
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|
ENST00000414678.7:c.3044T=
|
ENSP00000412835.2:p.Ile1015=
|
|
ENST00000635849.1:c.2207T=
|
ENSP00000490948.1:p.Ile736=
|
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ENST00000635957.1:c.1838T=
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ENSP00000490385.1:p.Ile613=
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ENST00000636227.1:n.3349T=
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ENST00000636254.1:n.806T=
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|
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ENST00000636930.2:c.4886T=
MANE Select
|
ENSP00000490491.2:p.Ile1629=
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ENST00000636940.1:n.2883T=
|
|
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ENST00000637015.1:c.2254T=
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ENST00000637568.1:c.2168T=
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ENST00000637741.1:n.1552T=
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|
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ENST00000637810.1:c.2228T=
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ENSP00000489636.1:p.Ile743=
|
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ENST00000637904.1:c.2387T=
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ENSP00000490550.1:p.Ile796=
|
|
ENST00000647938.1:c.4517T=
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ENSP00000498155.1:p.Ile1506=
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|
ENST00000346085.9:c.4517T=
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ENSP00000344546.4:p.Ile1506=
|
|
ENST00000350026.9:c.4478T=
|
ENSP00000055163.7:p.Ile1493=
|
|
ENST00000414678.6:c.3044T=
|
ENSP00000412835.2:p.Ile1015=
|
|
NM_017519.2:c.4478T=
|
NP_059989.2:p.Ile1493=
|
|
NM_020732.3:c.4517T=
|
NP_065783.3:p.Ile1506=
|
|
XM_005267069.3:c.4637T=
|
XP_005267126.2:p.Ile1546=
|
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XM_011535984.1:c.3716T=
|
XP_011534286.1:p.Ile1239=
|
|
XM_011535985.1:c.3536T=
|
XP_011534287.1:p.Ile1179=
|
|
XM_011535986.1:c.3296T=
|
XP_011534288.1:p.Ile1099=
|
|
XM_011535987.1:c.2915T=
|
XP_011534289.1:p.Ile972=
|
|
XM_011535988.1:c.1778T=
|
XP_011534290.1:p.Ile593=
|
|
NM_001346813.1:c.4637T=
|
NP_001333742.1:p.Ile1546=
|
|
NM_001363725.1:c.2387T=
|
NP_001350654.1:p.Ile796=
|
|
XM_011535984.2:c.4847T=
|
XP_011534286.2:p.Ile1616=
|
|
XM_011535988.3:c.1778T=
|
XP_011534290.1:p.Ile593=
|
|
XM_017011103.2:c.4748T=
|
XP_016866592.1:p.Ile1583=
|
|
XM_017011104.1:c.4718T=
|
XP_016866593.1:p.Ile1573=
|
|
XM_017011105.2:c.4688T=
|
XP_016866594.1:p.Ile1563=
|
|
XM_017011106.2:c.4559T=
|
XP_016866595.1:p.Ile1520=
|
|
XM_017011107.2:c.4538T=
|
XP_016866596.1:p.Ile1513=
|
|
XR_002956289.1:n.4833T=
|
|
|
NM_001363725.2:c.2387T=
|
NP_001350654.1:p.Ile796=
|
|
NM_001371656.1:c.4766T=
|
NP_001358585.1:p.Ile1589=
|
|
NM_001374820.1:c.4766T=
|
NP_001361749.1:p.Ile1589=
|
|
NM_001374828.1:c.4886T=
MANE Select
|
NP_001361757.1:p.Ile1629=
|
|
NM_017519.3:c.4727T=
|
NP_059989.3:p.Ile1576=
|
|