ENST00000502613.3:c.1187T>C
MANE Select
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ENSP00000424668.2:p.Val396Ala
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ENST00000335016.9:c.1187T>C
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ENSP00000334836.5:p.Val396Ala
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ENST00000389010.7:c.*163T>C
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ENSP00000373662.3:n.*163T>C
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ENST00000502613.1:c.264T>C
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|
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ENST00000502871.5:c.1187T>C
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ENSP00000421768.1:p.Val396Ala
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ENST00000505725.1:n.469T>C
|
|
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ENST00000628286.1:c.*163T>C
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ENSP00000487317.1:n.*163T>C
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NM_017593.3:c.1187T>C
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NP_060063.2:p.Val396Ala
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NM_198892.1:c.1187T>C
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NP_942595.1:p.Val396Ala
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XM_005263117.1:c.1187T>C
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XP_005263174.1:p.Val396Ala
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XM_011532101.1:c.947T>C
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XP_011530403.1:p.Val316Ala
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XM_011532102.1:c.1187T>C
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XP_011530404.1:p.Val396Ala
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XM_017008381.1:c.947T>C
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XP_016863870.1:p.Val316Ala
|
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XM_017008382.1:c.299T>C
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XP_016863871.1:p.Val100Ala
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NM_017593.4:c.1187T>C
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NP_060063.2:p.Val396Ala
|
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NM_017593.5:c.1187T>C
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NP_060063.2:p.Val396Ala
|
|
NM_198892.2:c.1187T>C
MANE Select
|
NP_942595.1:p.Val396Ala
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