ENST00000473665.2:n.5926A>G
|
|
|
ENST00000482662.2:n.4333A>G
|
|
|
ENST00000685865.1:n.2285A>G
|
|
|
ENST00000687250.1:n.1985A>G
|
|
|
ENST00000687995.1:n.1800A>G
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|
|
ENST00000688205.1:c.*1041A>G
|
ENSP00000509673.1:n.*1041A>G
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ENST00000688788.1:n.1687A>G
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|
|
ENST00000689276.1:c.1379A>G
|
ENSP00000510012.1:p.Asp460Gly
|
|
ENST00000689576.1:c.*67A>G
|
ENSP00000508712.1:n.*67A>G
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|
ENST00000690108.1:c.*1104A>G
|
ENSP00000510617.1:n.*1104A>G
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|
ENST00000690468.1:c.1017A>G
|
ENSP00000509078.1:p.Ter339Trp
|
|
ENST00000690595.1:c.773A>G
|
ENSP00000508979.1:p.Asp258Gly
|
|
ENST00000691348.1:c.1125A>G
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ENSP00000509369.1:p.Ter375Trp
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ENST00000691410.1:c.*1025A>G
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ENSP00000508479.1:n.*1025A>G
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|
ENST00000693287.1:c.764A>G
|
ENSP00000510264.1:p.Asp255Gly
|
|
ENST00000693681.1:c.761A>G
|
ENSP00000510789.1:p.Asp254Gly
|
|
ENST00000233838.9:c.1448A>G
MANE Select
|
ENSP00000233838.3:p.Asp483Gly
|
|
ENST00000233838.8:c.1448A>G
|
ENSP00000233838.3:p.Asp483Gly
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|
ENST00000430215.7:c.1277A>G
|
ENSP00000408045.3:p.Asp426Gly
|
|
ENST00000465637.5:n.179-3969A>G
|
|
|
NM_000821.5:c.1448A>G
|
NP_000812.2:p.Asp483Gly
|
|
NM_000821.6:c.1448A>G
|
NP_000812.2:p.Asp483Gly
|
|
NM_001142269.2:c.1277A>G
|
NP_001135741.1:p.Asp426Gly
|
|
NM_001142269.3:c.1277A>G
|
NP_001135741.1:p.Asp426Gly
|
|
XM_005264259.3:c.1448A>G
|
XP_005264316.1:p.Asp483Gly
|
|
XM_011532764.1:c.626A>G
|
XP_011531066.1:p.Asp209Gly
|
|
XM_011532765.1:c.626A>G
|
XP_011531067.1:p.Asp209Gly
|
|
XR_939677.1:n.1361A>G
|
|
|
XM_005264259.5:c.1448A>G
|
XP_005264316.1:p.Asp483Gly
|
|
XM_011532764.3:c.626A>G
|
XP_011531066.1:p.Asp209Gly
|
|
XM_011532765.3:c.626A>G
|
XP_011531067.1:p.Asp209Gly
|
|
XM_017003803.2:c.1277A>G
|
XP_016859292.1:p.Asp426Gly
|
|
XR_001738703.2:n.1361A>G
|
|
|
NM_000821.7:c.1448A>G
MANE Select
|
NP_000812.2:p.Asp483Gly
|
|
NM_001142269.4:c.1277A>G
|
NP_001135741.1:p.Asp426Gly
|
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