ENST00000324001.8:c.2126T>C
MANE Select
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ENSP00000326018.6:p.Val709Ala
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ENST00000673881.1:c.1709T>C
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ENSP00000501070.1:p.Val570Ala
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ENST00000674005.2:c.2411T>C
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ENSP00000501261.1:p.Val804Ala
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ENST00000674773.1:c.1709T>C
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ENSP00000502579.1:p.Val570Ala
|
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ENST00000675517.1:c.2001T>C
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|
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ENST00000676076.1:c.1987T>C
|
|
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ENST00000676260.1:c.2088T>C
|
|
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ENST00000676316.1:c.2013T>C
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|
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ENST00000291825.11:c.*2331T>C
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ENSP00000291825.6:n.*2331T>C
|
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ENST00000324001.7:c.2126T>C
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ENSP00000326018.6:p.Val709Ala
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NM_020956.2:c.*2331T>C , LRG_265t1:c.*2331T>C
|
NP_066007.1:n.*2331T>C
|
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NM_181882.2:c.2126T>C , LRG_265t2:c.2126T>C
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NP_870998.2:p.Val709Ala
|
|
XM_011527171.1:c.2126T>C
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XP_011525473.1:p.Val709Ala
|
|
XM_011527171.2:c.2126T>C
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XP_011525473.1:p.Val709Ala
|
|
XM_017027046.1:c.2024T>C
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XP_016882535.1:p.Val675Ala
|
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XM_017027047.1:c.2024T>C
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XP_016882536.1:p.Val675Ala
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NM_181882.3:c.2126T>C
MANE Select
|
NP_870998.2:p.Val709Ala
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