ENST00000326003.7:c.773T>G
MANE Select
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ENSP00000314151.1:p.Val258Gly
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ENST00000326003.6:c.773T>G
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ENSP00000314151.1:p.Val258Gly
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ENST00000360617.7:c.1215T>G
|
ENSP00000353829.2:n.1215T>G
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ENST00000422986.6:c.*429T>G
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ENSP00000393628.2:n.*429T>G
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ENST00000595392.5:c.*274T>G
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ENSP00000468912.1:n.*274T>G
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ENST00000595952.5:c.644T>G
|
ENSP00000471155.1:p.Val215Gly
|
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ENST00000596333.1:n.951T>G
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|
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ENST00000598145.1:c.775T>G
|
|
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ENST00000601349.5:n.2052T>G
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|
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ENST00000601812.1:n.1205T>G
|
|
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ENST00000617027.4:c.650T>G
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ENSP00000483513.1:p.Val217Gly
|
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NM_001030047.1:c.*498T>G
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NP_001025218.1:n.*498T>G
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NM_001030048.1:c.644T>G
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NP_001025219.1:p.Val215Gly
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NM_001648.2:c.773T>G
MANE Select
|
NP_001639.1:p.Val258Gly
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XM_011526923.1:c.791T>G
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XP_011525225.1:p.Val264Gly
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XR_935817.1:n.1324+860T>G
|
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