ENST00000330062.8:c.626T>G
MANE Select
|
ENSP00000331897.4:p.Val209Gly
|
|
ENST00000330062.7:c.626T>G
|
ENSP00000331897.3:p.Val209Gly
|
|
ENST00000540499.2:c.470T>G
|
ENSP00000446147.2:p.Val157Gly
|
|
ENST00000559482.5:c.299T>G
|
ENSP00000453016.1:p.Val100Gly
|
|
ENST00000560061.1:c.*251T>G
|
ENSP00000453254.1:n.*251T>G
|
|
NM_001289910.1:c.470T>G , LRG_611t1:c.470T>G
|
NP_001276839.1:p.Val157Gly
|
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NM_001290114.1:c.236T>G
|
NP_001277043.1:p.Val79Gly
|
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NM_002168.3:c.626T>G , LRG_611t2:c.626T>G
|
NP_002159.2:p.Val209Gly
|
|
NM_001290114.2:c.236T>G
|
NP_001277043.1:p.Val79Gly
|
|
NM_002168.4:c.626T>G
MANE Select
|
NP_002159.2:p.Val209Gly
|
|