ENST00000355808.10:c.917T>G
|
ENSP00000348062.6:p.Val306Gly
|
|
ENST00000379805.4:c.*588T>G
|
ENSP00000369133.3:n.*588T>G
|
|
ENST00000417819.6:c.980T>G
|
ENSP00000404616.2:p.Val327Gly
|
|
ENST00000423505.6:c.1010T>G
|
ENSP00000406473.2:p.Val337Gly
|
|
ENST00000481733.2:n.691T>G
|
|
|
ENST00000696704.1:c.*228T>G
|
ENSP00000512823.1:n.*228T>G
|
|
ENST00000696705.1:c.*351T>G
|
ENSP00000512824.1:n.*351T>G
|
|
ENST00000422285.7:c.896T>G
MANE Select
|
ENSP00000394382.2:p.Val299Gly
|
|
ENST00000379804.1:c.53T>G
|
ENSP00000369132.1:p.Val18Gly
|
|
ENST00000379806.9:c.1010T>G
|
ENSP00000369134.5:p.Val337Gly
|
|
ENST00000422285.6:c.896T>G
|
ENSP00000394382.2:p.Val299Gly
|
|
ENST00000478795.1:n.335T>G
|
|
|
ENST00000481733.1:n.324T>G
|
|
|
ENST00000540249.5:c.803T>G
|
ENSP00000440761.1:p.Val268Gly
|
|
ENST00000545074.5:c.917T>G
|
ENSP00000438550.1:p.Val306Gly
|
|
NM_000284.3:c.896T>G
|
NP_000275.1:p.Val299Gly
|
|
NM_001173454.1:c.1010T>G
|
NP_001166925.1:p.Val337Gly
|
|
NM_001173455.1:c.917T>G
|
NP_001166926.1:p.Val306Gly
|
|
NM_001173456.1:c.803T>G
|
NP_001166927.1:p.Val268Gly
|
|
XM_011545531.1:c.1031T>G
|
XP_011543833.1:p.Val344Gly
|
|
XM_011545532.1:c.938T>G
|
XP_011543834.1:p.Val313Gly
|
|
XM_017029574.2:c.917T>G
|
XP_016885063.1:p.Val306Gly
|
|
NM_000284.4:c.896T>G
MANE Select
|
NP_000275.1:p.Val299Gly
|
|
NM_001173454.2:c.1010T>G
|
NP_001166925.1:p.Val337Gly
|
|
NM_001173455.2:c.917T>G
|
NP_001166926.1:p.Val306Gly
|
|
NM_001173456.2:c.803T>G
|
NP_001166927.1:p.Val268Gly
|
|