ENST00000330062.8:c.541G>C
MANE Select
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ENSP00000331897.4:p.Ala181Pro
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ENST00000330062.7:c.541G>C
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ENSP00000331897.3:p.Ala181Pro
|
|
ENST00000540499.2:c.385G>C
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ENSP00000446147.2:p.Ala129Pro
|
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ENST00000559482.5:c.214G>C
|
ENSP00000453016.1:p.Ala72Pro
|
|
ENST00000560061.1:c.*166G>C
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ENSP00000453254.1:n.*166G>C
|
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NM_001289910.1:c.385G>C , LRG_611t1:c.385G>C
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NP_001276839.1:p.Ala129Pro
|
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NM_001290114.1:c.151G>C
|
NP_001277043.1:p.Ala51Pro
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NM_002168.3:c.541G>C , LRG_611t2:c.541G>C
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NP_002159.2:p.Ala181Pro
|
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NM_001290114.2:c.151G>C
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NP_001277043.1:p.Ala51Pro
|
|
NM_002168.4:c.541G>C
MANE Select
|
NP_002159.2:p.Ala181Pro
|
|