ENST00000318471.5:c.791A>G
MANE Select
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ENSP00000315680.3:p.Asp264Gly
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ENST00000541292.6:c.*56A>G
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ENSP00000441004.1:n.*56A>G
|
|
ENST00000678002.1:c.479A>G
|
|
|
ENST00000678557.1:c.677A>G
|
ENSP00000502962.1:p.Asp226Gly
|
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ENST00000678593.1:c.796A>G
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ENSP00000503841.1:n.796A>G
|
|
ENST00000679286.1:c.671A>G
|
ENSP00000503168.1:p.Asp224Gly
|
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ENST00000318471.4:c.791A>G
|
ENSP00000315680.3:p.Asp264Gly
|
|
NM_000288.3:c.791A>G
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NP_000279.1:p.Asp264Gly
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XM_005267019.3:c.677A>G
|
XP_005267076.1:p.Asp226Gly
|
|
XM_006715502.1:c.497A>G
|
XP_006715565.1:p.Asp166Gly
|
|
XM_011535900.1:c.527-25901A>G
|
XP_011534202.1:n.527-25901A>G
|
|
XM_005267019.4:c.677A>G
|
XP_005267076.1:p.Asp226Gly
|
|
XM_006715502.2:c.497A>G
|
XP_006715565.1:p.Asp166Gly
|
|
XM_017010934.2:c.527-25901A>G
|
XP_016866423.1:n.527-25901A>G
|
|
NM_000288.4:c.791A>G
MANE Select
|
NP_000279.1:p.Asp264Gly
|
|