ENST00000456935.7:c.387C>G
MANE Select
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ENSP00000395473.2:p.His129Gln
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ENST00000221363.8:c.387C>G
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ENSP00000221363.4:p.His129Gln
|
|
ENST00000456935.6:c.387C>G
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ENSP00000395473.2:p.His129Gln
|
|
ENST00000466794.5:n.369C>G
|
|
|
ENST00000486847.2:c.284C>G
|
ENSP00000470174.1:p.Thr95Ser
|
|
ENST00000596512.5:n.325C>G
|
|
|
ENST00000597961.1:c.378C>G
|
ENSP00000472710.1:p.His126Gln
|
|
ENST00000598876.1:c.414C>G
|
ENSP00000470533.1:p.His138Gln
|
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ENST00000600281.1:n.428C>G
|
|
|
NM_000528.3:c.387C>G
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NP_000519.2:p.His129Gln
|
|
NM_001173498.1:c.387C>G
|
NP_001166969.1:p.His129Gln
|
|
XM_005259913.1:c.387C>G
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XP_005259970.1:p.His129Gln
|
|
XM_005259913.2:c.387C>G
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XP_005259970.1:p.His129Gln
|
|
XM_024451518.1:c.-632C>G
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XP_024307286.1:n.-632C>G
|
|
NM_000528.4:c.387C>G
MANE Select
|
NP_000519.2:p.His129Gln
|
|
NM_001173498.2:c.387C>G
|
NP_001166969.1:p.His129Gln
|
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