ENST00000588860.6:c.982T=
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ENSP00000465878.2:p.Tyr328=
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|
ENST00000589076.6:c.982T=
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ENSP00000466934.2:p.Tyr328=
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ENST00000589941.2:c.982T=
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ENSP00000465874.2:p.Tyr328=
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|
ENST00000590061.2:c.982T=
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ENSP00000464772.2:p.Tyr328=
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ENST00000593223.2:c.982T=
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ENSP00000466118.2:p.Tyr328=
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|
ENST00000611848.2:c.982T=
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ENSP00000478613.2:p.Tyr328=
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ENST00000684953.1:n.2354T=
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|
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ENST00000685090.1:n.1433T=
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ENST00000685232.1:n.1090T=
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ENST00000688307.1:n.233T=
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ENST00000688574.1:n.1090T=
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|
|
ENST00000688903.1:n.1196T=
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|
|
ENST00000691124.1:n.2464T=
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|
|
ENST00000342988.8:c.982T=
MANE Select
|
ENSP00000341551.3:p.Tyr328=
|
|
ENST00000342988.7:c.982T=
|
ENSP00000341551.3:p.Tyr328=
|
|
ENST00000398417.6:c.982T=
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ENSP00000381452.1:p.Tyr328=
|
|
ENST00000588745.5:c.694T=
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ENSP00000464901.1:p.Tyr232=
|
|
ENST00000591126.5:n.2983T=
|
|
|
ENST00000592186.5:c.955+5533T=
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ENSP00000468611.1:n.955+5533T=
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|
ENST00000611848.1:c.182T=
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|
|
NM_005359.5:c.982T= , LRG_318t1:c.982T=
|
NP_005350.1:p.Tyr328=
|
|
NM_005359.6:c.982T=
MANE Select
|
NP_005350.1:p.Tyr328=
|
|