ENST00000261769.10:c.1755G=
MANE Select
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ENSP00000261769.4:p.Leu585=
|
|
ENST00000261769.9:c.1755G=
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ENSP00000261769.4:p.Leu585=
|
|
ENST00000422392.6:c.1572G=
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ENSP00000414946.2:p.Leu524=
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ENST00000562836.5:n.1826G=
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|
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ENST00000566510.5:c.*421G=
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ENSP00000458139.1:n.*421G=
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|
ENST00000566612.5:c.1609G=
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ENSP00000454782.1:p.Val537=
|
|
ENST00000611625.4:c.1818G=
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ENSP00000481063.1:p.Leu606=
|
|
ENST00000612417.4:c.1755G=
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ENSP00000478360.1:p.Leu585=
|
|
ENST00000621016.4:c.1755G=
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ENSP00000480664.1:p.Leu585=
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|
NM_004360.3:c.1755G= , LRG_301t1:c.1755G=
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NP_004351.1:p.Leu585=
|
|
XM_011523488.1:c.1020G=
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XP_011521790.1:p.Leu340=
|
|
XM_011523489.1:c.1020G=
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XP_011521791.1:p.Leu340=
|
|
NM_001317184.1:c.1572G=
|
NP_001304113.1:p.Leu524=
|
|
NM_001317185.1:c.207G=
|
NP_001304114.1:p.Leu69=
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|
NM_001317186.1:c.-211G=
|
NP_001304115.1:n.-211G=
|
|
NM_004360.4:c.1755G=
|
NP_004351.1:p.Leu585=
|
|
NM_004360.5:c.1755G=
MANE Select
|
NP_004351.1:p.Leu585=
|
|
NM_001317184.2:c.1572G=
|
NP_001304113.1:p.Leu524=
|
|
NM_001317185.2:c.207G=
|
NP_001304114.1:p.Leu69=
|
|
NM_001317186.2:c.-211G=
|
NP_001304115.1:n.-211G=
|
|