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ENST00000261769.10:c.2362G=
MANE Select
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ENSP00000261769.4:p.Ala788=
|
|
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ENST00000261769.9:c.2362G=
|
ENSP00000261769.4:p.Ala788=
|
|
|
ENST00000422392.6:c.2179G=
|
ENSP00000414946.2:p.Ala727=
|
|
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ENST00000562118.1:n.580G=
|
|
|
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ENST00000562836.5:n.2433G=
|
|
|
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ENST00000566510.5:c.*1028G=
|
ENSP00000458139.1:n.*1028G=
|
|
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ENST00000566612.5:c.*602G=
|
ENSP00000454782.1:n.*602G=
|
|
|
ENST00000611625.4:c.2425G=
|
ENSP00000481063.1:p.Ala809=
|
|
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ENST00000612417.4:c.1853+3166G=
|
ENSP00000478360.1:n.1853+3166G=
|
|
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ENST00000621016.4:c.1866-4483G=
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ENSP00000480664.1:n.1866-4483G=
|
|
|
NM_004360.3:c.2362G= , LRG_301t1:c.2362G=
|
NP_004351.1:p.Ala788=
|
|
|
XM_011523488.1:c.1627G=
|
XP_011521790.1:p.Ala543=
|
|
|
XM_011523489.1:c.1627G=
|
XP_011521791.1:p.Ala543=
|
|
|
NM_001317184.1:c.2179G=
|
NP_001304113.1:p.Ala727=
|
|
|
NM_001317185.1:c.814G=
|
NP_001304114.1:p.Ala272=
|
|
|
NM_001317186.1:c.397G=
|
NP_001304115.1:p.Ala133=
|
|
|
NM_004360.4:c.2362G=
|
NP_004351.1:p.Ala788=
|
|
|
NM_004360.5:c.2362G=
MANE Select
|
NP_004351.1:p.Ala788=
|
|
|
NM_001317184.2:c.2179G=
|
NP_001304113.1:p.Ala727=
|
|
|
NM_001317185.2:c.814G=
|
NP_001304114.1:p.Ala272=
|
|
|
NM_001317186.2:c.397G=
|
NP_001304115.1:p.Ala133=
|
|
