ENST00000355773.6:c.1330G>A
MANE Select
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ENSP00000348019.5:p.Ala444Thr
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ENST00000355773.5:c.1330G>A
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ENSP00000348019.5:p.Ala444Thr
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|
NM_012434.4:c.1330G>A
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NP_036566.1:p.Ala444Thr
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XM_005248710.2:c.1279G>A
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XP_005248767.1:p.Ala427Thr
|
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XM_005248711.1:c.1132G>A
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XP_005248768.1:p.Ala378Thr
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XM_011535750.1:c.1182G>A
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XP_011534052.1:p.Leu394=
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|
NM_012434.5:c.1330G>A
MANE Select
|
NP_036566.1:p.Ala444Thr
|
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NM_001382629.1:c.1099G>A
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NP_001369558.1:p.Ala367Thr
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NM_001382630.1:c.1260-5157G>A
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NP_001369559.1:n.1260-5157G>A
|
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NM_001382631.1:c.1351G>A
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NP_001369560.1:p.Ala451Thr
|
|
NM_001382632.1:c.1243G>A
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NP_001369561.1:p.Ala415Thr
|
|
NM_001382633.1:c.1330G>A
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NP_001369562.1:p.Ala444Thr
|
|
NM_001382634.1:c.1171G>A
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NP_001369563.1:p.Ala391Thr
|
|
NM_001382635.1:c.1327G>A
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NP_001369564.1:p.Ala443Thr
|
|
NM_001382636.1:c.1012G>A
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NP_001369565.1:p.Ala338Thr
|
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