ENST00000261769.10:c.1975G>T
MANE Select
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ENSP00000261769.4:p.Glu659Ter
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ENST00000261769.9:c.1975G>T
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ENSP00000261769.4:p.Glu659Ter
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ENST00000422392.6:c.1792G>T
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ENSP00000414946.2:p.Glu598Ter
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ENST00000562118.1:n.193G>T
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|
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ENST00000562836.5:n.2046G>T
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|
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ENST00000566510.5:c.*641G>T
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ENSP00000458139.1:n.*641G>T
|
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ENST00000566612.5:c.*215G>T
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ENSP00000454782.1:n.*215G>T
|
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ENST00000611625.4:c.2038G>T
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ENSP00000481063.1:p.Glu680Ter
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ENST00000612417.4:c.1830+1318G>T
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ENSP00000478360.1:n.1830+1318G>T
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ENST00000621016.4:c.1865+1283G>T
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ENSP00000480664.1:n.1865+1283G>T
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NM_004360.3:c.1975G>T , LRG_301t1:c.1975G>T
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NP_004351.1:p.Glu659Ter
|
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XM_011523488.1:c.1240G>T
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XP_011521790.1:p.Glu414Ter
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XM_011523489.1:c.1240G>T
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XP_011521791.1:p.Glu414Ter
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NM_001317184.1:c.1792G>T
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NP_001304113.1:p.Glu598Ter
|
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NM_001317185.1:c.427G>T
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NP_001304114.1:p.Glu143Ter
|
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NM_001317186.1:c.10G>T
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NP_001304115.1:p.Glu4Ter
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NM_004360.4:c.1975G>T
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NP_004351.1:p.Glu659Ter
|
|
NM_004360.5:c.1975G>T
MANE Select
|
NP_004351.1:p.Glu659Ter
|
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NM_001317184.2:c.1792G>T
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NP_001304113.1:p.Glu598Ter
|
|
NM_001317185.2:c.427G>T
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NP_001304114.1:p.Glu143Ter
|
|
NM_001317186.2:c.10G>T
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NP_001304115.1:p.Glu4Ter
|
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