ENST00000355773.6:c.505G>A
MANE Select
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ENSP00000348019.5:p.Ala169Thr
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ENST00000355773.5:c.505G>A
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ENSP00000348019.5:p.Ala169Thr
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ENST00000481996.1:n.271G>A
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|
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NM_012434.4:c.505G>A
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NP_036566.1:p.Ala169Thr
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XM_005248710.2:c.454G>A
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XP_005248767.1:p.Ala152Thr
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XM_005248711.1:c.307G>A
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XP_005248768.1:p.Ala103Thr
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XM_011535750.1:c.505G>A
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XP_011534052.1:p.Ala169Thr
|
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XM_011535751.1:c.505G>A
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XP_011534053.1:p.Ala169Thr
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NM_012434.5:c.505G>A
MANE Select
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NP_036566.1:p.Ala169Thr
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NM_001382629.1:c.274G>A
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NP_001369558.1:p.Ala92Thr
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NM_001382630.1:c.505G>A
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NP_001369559.1:p.Ala169Thr
|
|
NM_001382631.1:c.526G>A
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NP_001369560.1:p.Ala176Thr
|
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NM_001382632.1:c.505G>A
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NP_001369561.1:p.Ala169Thr
|
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NM_001382633.1:c.505G>A
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NP_001369562.1:p.Ala169Thr
|
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NM_001382634.1:c.505G>A
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NP_001369563.1:p.Ala169Thr
|
|
NM_001382635.1:c.505G>A
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NP_001369564.1:p.Ala169Thr
|
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NM_001382636.1:c.274G>A
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NP_001369565.1:p.Ala92Thr
|
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