ENST00000261769.10:c.2581T=
MANE Select
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ENSP00000261769.4:p.Tyr861=
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ENST00000261769.9:c.2581T=
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ENSP00000261769.4:p.Tyr861=
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ENST00000422392.6:c.2398T=
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ENSP00000414946.2:p.Tyr800=
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ENST00000562118.1:n.799T=
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|
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ENST00000562836.5:n.2652T=
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|
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ENST00000566510.5:c.*1247T=
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ENSP00000458139.1:n.*1247T=
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ENST00000566612.5:c.*821T=
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ENSP00000454782.1:n.*821T=
|
|
ENST00000611625.4:c.2644T=
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ENSP00000481063.1:p.Tyr882=
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ENST00000612417.4:c.1854-760T=
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ENSP00000478360.1:n.1854-760T=
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ENST00000621016.4:c.1866-772T=
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ENSP00000480664.1:n.1866-772T=
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NM_004360.3:c.2581T= , LRG_301t1:c.2581T=
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NP_004351.1:p.Tyr861=
|
|
XM_011523488.1:c.1846T=
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XP_011521790.1:p.Tyr616=
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XM_011523489.1:c.1846T=
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XP_011521791.1:p.Tyr616=
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NM_001317184.1:c.2398T=
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NP_001304113.1:p.Tyr800=
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|
NM_001317185.1:c.1033T=
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NP_001304114.1:p.Tyr345=
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|
NM_001317186.1:c.616T=
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NP_001304115.1:p.Tyr206=
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|
NM_004360.4:c.2581T=
|
NP_004351.1:p.Tyr861=
|
|
NM_004360.5:c.2581T=
MANE Select
|
NP_004351.1:p.Tyr861=
|
|
NM_001317184.2:c.2398T=
|
NP_001304113.1:p.Tyr800=
|
|
NM_001317185.2:c.1033T=
|
NP_001304114.1:p.Tyr345=
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|
NM_001317186.2:c.616T=
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NP_001304115.1:p.Tyr206=
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