ENST00000403665.7:c.1195T=
MANE Select
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ENSP00000384957.2:p.Trp399=
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|
ENST00000264692.8:c.1033T=
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ENSP00000264692.5:p.Trp345=
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|
ENST00000403665.6:c.1195T=
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ENSP00000384957.2:p.Trp399=
|
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NM_000128.3:c.1195T= , LRG_583t1:c.1195T=
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NP_000119.1:p.Trp399=
|
|
XM_005262821.2:c.1198T=
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XP_005262878.1:p.Trp400=
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|
XM_005262822.2:c.1198T=
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XP_005262879.1:p.Trp400=
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|
XM_005262823.2:c.928T=
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XP_005262880.1:p.Trp310=
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|
XM_005262824.1:c.1198T=
|
XP_005262881.1:p.Trp400=
|
|
XM_006714137.1:c.1150T=
|
XP_006714200.1:p.Trp384=
|
|
XR_938706.1:n.1603T=
|
|
|
XR_938707.1:n.1603T=
|
|
|
XM_005262821.4:c.1198T=
|
XP_005262878.1:p.Trp400=
|
|
XM_005262822.4:c.1198T=
|
XP_005262879.1:p.Trp400=
|
|
XM_005262823.4:c.928T=
|
XP_005262880.1:p.Trp310=
|
|
XM_006714137.3:c.1150T=
|
XP_006714200.1:p.Trp384=
|
|
XM_017007884.2:c.*2167T=
|
XP_016863373.1:n.*2167T=
|
|
XM_017007885.2:c.*63T=
|
XP_016863374.1:n.*63T=
|
|
XR_001741172.2:n.1669T=
|
|
|
NM_000128.4:c.1195T=
MANE Select
|
NP_000119.1:p.Trp399=
|
|