ENST00000355943.8:c.386T>G
MANE Select
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ENSP00000348211.3:p.Val129Gly
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ENST00000355943.7:c.386T>G
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ENSP00000348211.3:p.Val129Gly
|
|
ENST00000447245.6:c.386T>G
|
ENSP00000399717.2:p.Val129Gly
|
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ENST00000502462.6:n.702T>G
|
|
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ENST00000504098.1:c.-53T>G
|
ENSP00000425708.1:n.-53T>G
|
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ENST00000508781.5:n.215T>G
|
|
|
ENST00000513807.5:c.-101T>G
|
ENSP00000421134.1:n.-101T>G
|
|
NM_001303249.1:c.386T>G
|
NP_001290178.1:p.Val129Gly
|
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NM_001303250.1:c.113T>G
|
NP_001290179.1:p.Val38Gly
|
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NM_138773.2:c.386T>G
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NP_620128.1:p.Val129Gly
|
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XM_011543708.1:c.386T>G
|
XP_011542010.1:p.Val129Gly
|
|
NM_001303249.2:c.386T>G
|
NP_001290178.1:p.Val129Gly
|
|
NM_001303250.2:c.113T>G
|
NP_001290179.1:p.Val38Gly
|
|
NM_138773.3:c.386T>G
|
NP_620128.1:p.Val129Gly
|
|
NR_138151.1:n.534T>G
|
|
|
NM_138773.4:c.386T>G
MANE Select
|
NP_620128.1:p.Val129Gly
|
|
NM_001303249.3:c.386T>G
|
NP_001290178.1:p.Val129Gly
|
|
NM_001303250.3:c.113T>G
|
NP_001290179.1:p.Val38Gly
|
|
NR_138151.2:n.499T>G
|
|
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