ENST00000252826.10:c.8T>G
MANE Select
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ENSP00000252826.4:p.Val3Gly
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ENST00000252826.9:c.8T>G
|
ENSP00000252826.4:p.Val3Gly
|
|
ENST00000427978.6:c.8T>G
|
ENSP00000407492.1:p.Val3Gly
|
|
ENST00000595519.5:c.8T>G
|
ENSP00000469893.1:p.Val3Gly
|
|
ENST00000596338.5:n.43T>G
|
|
|
ENST00000598502.5:c.8T>G
|
ENSP00000470229.1:p.Val3Gly
|
|
ENST00000598691.5:c.8T>G
|
ENSP00000473231.1:p.Val3Gly
|
|
ENST00000598697.5:c.8T>G
|
ENSP00000468989.1:p.Val3Gly
|
|
ENST00000599628.5:c.8T>G
|
ENSP00000483753.1:p.Val3Gly
|
|
NM_001195227.1:c.8T>G
|
NP_001182156.1:p.Val3Gly
|
|
NM_017636.3:c.8T>G
|
NP_060106.2:p.Val3Gly
|
|
XM_011527046.1:c.-159T>G
|
XP_011525348.1:n.-159T>G
|
|
NM_001321281.1:c.8T>G
|
NP_001308210.1:p.Val3Gly
|
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NM_001321282.1:c.-1365T>G
|
NP_001308211.1:n.-1365T>G
|
|
NM_001321283.1:c.-159T>G
|
NP_001308212.1:n.-159T>G
|
|
NM_001321285.1:c.-322T>G
|
NP_001308214.1:n.-322T>G
|
|
NM_017636.4:c.8T>G
MANE Select
|
NP_060106.2:p.Val3Gly
|
|
NM_001195227.2:c.8T>G
|
NP_001182156.1:p.Val3Gly
|
|
NM_001321281.2:c.8T>G
|
NP_001308210.1:p.Val3Gly
|
|
NM_001321282.2:c.-1365T>G
|
NP_001308211.1:n.-1365T>G
|
|
NM_001321283.2:c.-159T>G
|
NP_001308212.1:n.-159T>G
|
|
NM_001321285.2:c.-322T>G
|
NP_001308214.1:n.-322T>G
|
|