ENST00000326003.7:c.347A>G
MANE Select
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ENSP00000314151.1:p.Asp116Gly
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ENST00000326003.6:c.347A>G
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ENSP00000314151.1:p.Asp116Gly
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ENST00000360617.7:c.347A>G
|
ENSP00000353829.2:p.Asp116Gly
|
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ENST00000422986.6:c.*3A>G
|
ENSP00000393628.2:n.*3A>G
|
|
ENST00000593997.5:c.347A>G
|
ENSP00000472907.1:p.Asp116Gly
|
|
ENST00000595392.5:c.347A>G
|
ENSP00000468912.1:p.Asp116Gly
|
|
ENST00000595952.5:c.218A>G
|
ENSP00000471155.1:p.Asp73Gly
|
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ENST00000596185.5:c.*455A>G
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ENSP00000471648.1:n.*455A>G
|
|
ENST00000596333.1:n.382A>G
|
|
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ENST00000597286.5:c.236A>G
|
ENSP00000470523.1:p.Asp79Gly
|
|
ENST00000597483.5:c.218A>G
|
ENSP00000472411.1:p.Asp73Gly
|
|
ENST00000598145.1:c.331A>G
|
|
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ENST00000601349.5:n.1626A>G
|
|
|
ENST00000601503.5:c.290A>G
|
ENSP00000472213.1:p.Asp97Gly
|
|
ENST00000601812.1:n.779A>G
|
|
|
ENST00000617027.4:c.347A>G
|
ENSP00000483513.1:p.Asp116Gly
|
|
NM_001030047.1:c.347A>G
|
NP_001025218.1:p.Asp116Gly
|
|
NM_001030048.1:c.218A>G
|
NP_001025219.1:p.Asp73Gly
|
|
NM_001648.2:c.347A>G
MANE Select
|
NP_001639.1:p.Asp116Gly
|
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XM_011526923.1:c.347A>G
|
XP_011525225.1:p.Asp116Gly
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|
XM_011526924.1:c.347A>G
|
XP_011525226.1:p.Asp116Gly
|
|
XR_935817.1:n.382A>G
|
|
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