ENST00000395925.8:c.2239_2242delinsACCC
MANE Select
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ENSP00000379258.3:p.Thr747=
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|
ENST00000677288.1:c.2065_2068delinsACCC
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ENSP00000503986.1:p.Thr689=
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|
ENST00000677605.1:c.2239_2242delinsACCC
|
ENSP00000503743.1:p.Thr747=
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ENST00000678429.1:c.2239_2242delinsACCC
|
ENSP00000502957.1:p.Thr747=
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|
ENST00000395925.7:c.2239_2242delinsACCC
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ENSP00000379258.3:p.Thr747=
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|
ENST00000479210.1:n.2216_2219delinsACCC
|
|
|
NM_000168.5:c.2239_2242delinsACCC
|
NP_000159.3:p.Thr747=
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|
XM_005249703.1:c.2239_2242delinsACCC
|
XP_005249760.1:p.Thr747=
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|
XM_005249704.2:c.2239_2242delinsACCC
|
XP_005249761.1:p.Thr747=
|
|
XM_011515272.1:c.2239_2242delinsACCC
|
XP_011513574.1:p.Thr747=
|
|
XM_011515273.1:c.2239_2242delinsACCC
|
XP_011513575.1:p.Thr747=
|
|
XM_011515274.1:c.2062_2065delinsACCC
|
XP_011513576.1:p.Thr688=
|
|
XM_011515274.2:c.2062_2065delinsACCC
|
XP_011513576.1:p.Thr688=
|
|
XM_017011997.1:c.2236_2239delinsACCC
|
XP_016867486.1:p.Thr746=
|
|
NM_000168.6:c.2239_2242delinsACCC
MANE Select
|
NP_000159.3:p.Thr747=
|
|