ENST00000330062.8:c.583G>T
MANE Select
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ENSP00000331897.4:p.Val195Phe
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ENST00000330062.7:c.583G>T
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ENSP00000331897.3:p.Val195Phe
|
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ENST00000540499.2:c.427G>T
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ENSP00000446147.2:p.Val143Phe
|
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ENST00000559482.5:c.256G>T
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ENSP00000453016.1:p.Val86Phe
|
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ENST00000560061.1:c.*208G>T
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ENSP00000453254.1:n.*208G>T
|
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NM_001289910.1:c.427G>T , LRG_611t1:c.427G>T
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NP_001276839.1:p.Val143Phe
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NM_001290114.1:c.193G>T
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NP_001277043.1:p.Val65Phe
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NM_002168.3:c.583G>T , LRG_611t2:c.583G>T
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NP_002159.2:p.Val195Phe
|
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NM_001290114.2:c.193G>T
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NP_001277043.1:p.Val65Phe
|
|
NM_002168.4:c.583G>T
MANE Select
|
NP_002159.2:p.Val195Phe
|
|