ENST00000396705.10:c.643G>A
MANE Select
|
ENSP00000379933.4:p.Gly215Arg
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ENST00000229270.8:c.754G>A
|
ENSP00000229270.4:p.Gly252Arg
|
|
ENST00000396705.9:c.643G>A
|
ENSP00000379933.4:p.Gly215Arg
|
|
ENST00000474253.1:n.132G>A
|
|
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ENST00000488464.6:c.397G>A
|
ENSP00000475620.1:p.Gly133Arg
|
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ENST00000535434.5:c.397G>A
|
ENSP00000443599.1:p.Gly133Arg
|
|
ENST00000613953.4:c.754G>A
|
ENSP00000484435.1:p.Gly252Arg
|
|
NM_000365.5:c.643G>A
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NP_000356.1:p.Gly215Arg
|
|
NM_001159287.1:c.754G>A
|
NP_001152759.1:p.Gly252Arg
|
|
NM_001258026.1:c.397G>A
|
NP_001244955.1:p.Gly133Arg
|
|
XR_002957378.1:n.1651G>A
|
|
|
NM_000365.6:c.643G>A
MANE Select
|
NP_000356.1:p.Gly215Arg
|
|
NM_001258026.2:c.397G>A
|
NP_001244955.1:p.Gly133Arg
|
|