ENST00000297784.10:c.1913G>T
MANE Select
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ENSP00000297784.6:p.Gly638Val
|
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ENST00000644967.1:c.*353G>T
|
ENSP00000496159.1:n.*353G>T
|
|
ENST00000645053.1:c.1258-5878G>T
|
ENSP00000493838.1:n.1258-5878G>T
|
|
ENST00000645208.2:c.1913G>T
|
ENSP00000494684.1:p.Gly638Val
|
|
ENST00000645773.1:c.1787G>T
|
ENSP00000493698.1:p.Gly596Val
|
|
ENST00000645787.1:n.2056G>T
|
|
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ENST00000646619.1:c.1475G>T
|
ENSP00000493726.1:p.Gly492Val
|
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ENST00000651183.1:c.1475G>T
|
ENSP00000498723.1:p.Gly492Val
|
|
ENST00000297784.9:c.1913G>T
|
ENSP00000297784.5:p.Gly638Val
|
|
ENST00000340019.4:c.1913G>T
|
ENSP00000341433.3:p.Gly638Val
|
|
ENST00000469455.1:n.394G>T
|
|
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ENST00000486417.5:n.811G>T
|
|
|
NM_138691.2:c.1913G>T
|
NP_619636.2:p.Gly638Val
|
|
XM_011518213.1:c.2501G>T
|
XP_011516515.1:p.Gly834Val
|
|
XM_017014256.1:c.1916G>T
|
XP_016869745.1:p.Gly639Val
|
|
NM_138691.3:c.1913G>T
MANE Select
|
NP_619636.2:p.Gly638Val
|
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