ENST00000409709.9:c.*141A>C
MANE Select
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ENSP00000386331.3:n.*141A>C
|
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ENST00000670577.1:c.4590A>C
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|
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ENST00000409619.6:c.*141A>C
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ENSP00000386635.2:n.*141A>C
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ENST00000409709.7:c.*141A>C
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ENSP00000386331.3:n.*141A>C
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ENST00000458169.2:c.4215A>C
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ENSP00000417017.2:n.4215A>C
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ENST00000458637.6:c.*141A>C
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ENSP00000392185.2:n.*141A>C
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ENST00000481328.7:n.5339A>C
|
|
|
ENST00000605744.1:n.2303A>C
|
|
|
NM_000260.3:c.*141A>C
|
NP_000251.3:n.*141A>C
|
|
NM_001127180.1:c.*141A>C
|
NP_001120652.1:n.*141A>C
|
|
XM_005274012.2:c.*141A>C
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XP_005274069.1:n.*141A>C
|
|
XM_006718561.2:c.*141A>C
|
XP_006718624.1:n.*141A>C
|
|
XR_949941.1:n.7083A>C
|
|
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XM_017017780.1:c.*141A>C
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XP_016873269.1:n.*141A>C
|
|
XM_017017784.1:c.*141A>C
|
XP_016873273.1:n.*141A>C
|
|
XM_017017788.1:c.*141A>C
|
XP_016873277.1:n.*141A>C
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|
XR_001747885.1:n.6868A>C
|
|
|
XR_001747887.1:n.6854A>C
|
|
|
NM_000260.4:c.*141A>C
MANE Select
|
NP_000251.3:n.*141A>C
|
|
NM_001127180.2:c.*141A>C
|
NP_001120652.1:n.*141A>C
|
|
NM_001369365.1:c.*141A>C
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NP_001356294.1:n.*141A>C
|
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