ENST00000261769.10:c.2584T=
MANE Select
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ENSP00000261769.4:p.Leu862=
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ENST00000261769.9:c.2584T=
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ENSP00000261769.4:p.Leu862=
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ENST00000422392.6:c.2401T=
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ENSP00000414946.2:p.Leu801=
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ENST00000562118.1:n.802T=
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|
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ENST00000562836.5:n.2655T=
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|
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ENST00000566510.5:c.*1250T=
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ENSP00000458139.1:n.*1250T=
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|
ENST00000566612.5:c.*824T=
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ENSP00000454782.1:n.*824T=
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ENST00000611625.4:c.2647T=
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ENSP00000481063.1:p.Leu883=
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ENST00000612417.4:c.1854-757T=
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ENSP00000478360.1:n.1854-757T=
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ENST00000621016.4:c.1866-769T=
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ENSP00000480664.1:n.1866-769T=
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NM_004360.3:c.2584T= , LRG_301t1:c.2584T=
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NP_004351.1:p.Leu862=
|
|
XM_011523488.1:c.1849T=
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XP_011521790.1:p.Leu617=
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XM_011523489.1:c.1849T=
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XP_011521791.1:p.Leu617=
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NM_001317184.1:c.2401T=
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NP_001304113.1:p.Leu801=
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NM_001317185.1:c.1036T=
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NP_001304114.1:p.Leu346=
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|
NM_001317186.1:c.619T=
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NP_001304115.1:p.Leu207=
|
|
NM_004360.4:c.2584T=
|
NP_004351.1:p.Leu862=
|
|
NM_004360.5:c.2584T=
MANE Select
|
NP_004351.1:p.Leu862=
|
|
NM_001317184.2:c.2401T=
|
NP_001304113.1:p.Leu801=
|
|
NM_001317185.2:c.1036T=
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NP_001304114.1:p.Leu346=
|
|
NM_001317186.2:c.619T=
|
NP_001304115.1:p.Leu207=
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