ENST00000405460.9:c.11509G=
MANE Select
|
ENSP00000384582.2:p.Val3837=
|
|
ENST00000425867.3:c.640G=
|
ENSP00000392618.3:p.Val214=
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|
ENST00000639431.1:c.265+78905G=
|
ENSP00000491057.1:n.265+78905G=
|
|
ENST00000640374.1:n.4653G=
|
|
|
ENST00000640464.1:n.1928G=
|
|
|
ENST00000405460.6:c.11509G=
|
ENSP00000384582.2:p.Val3837=
|
|
ENST00000509621.1:c.4206G=
|
|
|
NM_032119.3:c.11509G=
|
NP_115495.3:p.Val3837=
|
|
NR_003149.1:n.11522G=
|
|
|
XM_011543675.1:c.11506G=
|
XP_011541977.1:p.Val3836=
|
|
XM_011543676.1:c.11428G=
|
XP_011541978.1:p.Val3810=
|
|
XM_011543677.1:c.8812G=
|
XP_011541979.1:p.Val2938=
|
|
XM_011543678.1:c.11509G=
|
XP_011541980.1:p.Val3837=
|
|
NM_032119.4:c.11509G=
MANE Select
|
NP_115495.3:p.Val3837=
|
|
XM_017009963.2:c.11530G=
|
XP_016865452.1:p.Val3844=
|
|
XM_017009964.2:c.11527G=
|
XP_016865453.1:p.Val3843=
|
|
XM_017009965.1:c.11527G=
|
XP_016865454.1:p.Val3843=
|
|
XM_017009966.2:c.11449G=
|
XP_016865455.1:p.Val3817=
|
|
XM_017009967.1:c.11434G=
|
XP_016865456.1:p.Val3812=
|
|
XM_017009968.2:c.11530G=
|
XP_016865457.1:p.Val3844=
|
|
XM_017009969.2:c.11530G=
|
XP_016865458.1:p.Val3844=
|
|
XM_017009970.2:c.11530G=
|
XP_016865459.1:p.Val3844=
|
|
XM_017009971.2:c.11530G=
|
XP_016865460.1:p.Val3844=
|
|
XM_017009972.1:c.4648G=
|
XP_016865461.1:p.Val1550=
|
|
XM_017009973.1:c.4627G=
|
XP_016865462.1:p.Val1543=
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|
NR_003149.2:n.11525G=
|
|
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