ENST00000290866.10:c.2326A=
MANE Select
|
ENSP00000290866.4:p.Thr776=
|
|
ENST00000290863.10:c.604A=
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ENSP00000290863.6:p.Thr202=
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ENST00000290866.9:c.2326A=
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ENSP00000290866.4:p.Thr776=
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ENST00000413513.7:c.604A=
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ENSP00000392247.3:p.Thr202=
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|
ENST00000428043.5:c.2326A=
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ENSP00000397593.2:p.Thr776=
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|
ENST00000577647.2:c.604A=
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ENSP00000464149.1:p.Thr202=
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ENST00000578839.5:c.*396A=
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ENSP00000462110.2:n.*396A=
|
|
ENST00000579204.1:c.585A=
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ENSP00000464629.1:n.585A=
|
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ENST00000579314.5:c.*55A=
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ENSP00000462599.1:n.*55A=
|
|
ENST00000582005.5:c.*246A=
|
ENSP00000462002.1:n.*246A=
|
|
ENST00000582761.1:c.94A=
|
ENSP00000462909.1:p.Thr32=
|
|
ENST00000584865.5:n.272A=
|
|
|
NM_000789.3:c.2326A=
|
NP_000780.1:p.Thr776=
|
|
NM_001178057.1:c.604A=
|
NP_001171528.1:p.Thr202=
|
|
NM_152830.2:c.604A=
|
NP_690043.1:p.Thr202=
|
|
XM_005257110.1:c.1777A=
|
XP_005257167.1:p.Thr593=
|
|
XM_006721737.2:c.664A=
|
XP_006721800.2:p.Thr222=
|
|
XM_006721737.3:c.664A=
|
XP_006721800.2:p.Thr222=
|
|
NM_000789.4:c.2326A=
MANE Select
|
NP_000780.1:p.Thr776=
|
|
NM_001178057.2:c.604A=
|
NP_001171528.1:p.Thr202=
|
|
NM_152830.3:c.604A=
|
NP_690043.1:p.Thr202=
|
|
NM_001382700.1:c.1759A=
|
NP_001369629.1:p.Thr587=
|
|
NM_001382701.1:c.1474A=
|
NP_001369630.1:p.Thr492=
|
|
NM_001382702.1:c.256A=
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NP_001369631.1:p.Thr86=
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|
NR_168483.1:n.704A=
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|
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