ENST00000682275.1:c.2397T=
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ENSP00000507852.1:p.Ala799=
|
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ENST00000683395.1:c.2338T=
|
|
|
ENST00000684087.1:c.2361T=
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ENSP00000506978.1:p.Ala787=
|
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ENST00000506362.2:c.2112T=
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ENSP00000424103.2:p.Ala704=
|
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ENST00000673991.1:c.2397T=
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ENSP00000501033.1:p.Ala799=
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ENST00000226760.5:c.2361T=
MANE Select
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ENSP00000226760.1:p.Ala787=
|
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ENST00000503569.5:c.2361T=
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ENSP00000423337.1:p.Ala787=
|
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ENST00000507765.1:n.2546T=
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|
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NM_001145853.1:c.2361T=
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NP_001139325.1:p.Ala787=
|
|
NM_006005.3:c.2361T=
MANE Select
|
NP_005996.2:p.Ala787=
|
|
XM_017008586.1:c.2370T=
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XP_016864075.1:p.Ala790=
|
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