ENST00000686073.1:c.1101A>T
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ENSP00000508901.1:p.Ala367=
|
|
ENST00000380993.8:c.1101A>T
MANE Select
|
ENSP00000370381.3:p.Ala367=
|
|
ENST00000646012.1:c.1239A>T
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ENSP00000495813.1:p.Ala413=
|
|
ENST00000647232.1:c.1101A>T
|
ENSP00000493875.1:p.Ala367=
|
|
ENST00000647546.1:c.1101A>T
|
ENSP00000495332.1:p.Ala367=
|
|
ENST00000330289.10:c.1101A>T
|
ENSP00000331550.6:p.Ala367=
|
|
ENST00000380993.7:c.1101A>T
|
ENSP00000370381.3:p.Ala367=
|
|
ENST00000396577.7:c.1101A>T
|
ENSP00000379822.3:p.Ala367=
|
|
ENST00000558252.5:n.5224A>T
|
|
|
ENST00000558405.5:c.1101A>T
|
ENSP00000453409.1:p.Ala367=
|
|
ENST00000558805.1:c.128A>T
|
|
|
ENST00000559641.5:c.540A>T
|
ENSP00000453230.1:p.Ala180=
|
|
ENST00000559723.2:n.474A>T
|
|
|
ENST00000560692.5:n.5240A>T
|
|
|
NM_000338.2:c.1101A>T
|
NP_000329.2:p.Ala367=
|
|
NM_001184832.1:c.1101A>T
|
NP_001171761.1:p.Ala367=
|
|
XM_005254605.1:c.1197A>T
|
XP_005254662.1:p.Ala399=
|
|
XM_005254606.1:c.1101A>T
|
XP_005254663.1:p.Ala367=
|
|
XM_006720656.1:c.1197A>T
|
XP_006720719.1:p.Ala399=
|
|
XR_931896.1:n.1413A>T
|
|
|
XM_005254606.2:c.1101A>T
|
XP_005254663.1:p.Ala367=
|
|
NM_000338.3:c.1101A>T
MANE Select
|
NP_000329.2:p.Ala367=
|
|
NM_001184832.2:c.1101A>T
|
NP_001171761.1:p.Ala367=
|
|
NM_001384136.1:c.1101A>T
|
NP_001371065.1:p.Ala367=
|
|