ENST00000324001.8:c.2177A>T
MANE Select
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ENSP00000326018.6:p.Glu726Val
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ENST00000673881.1:c.1760A>T
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ENSP00000501070.1:p.Glu587Val
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ENST00000674005.2:c.2462A>T
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ENSP00000501261.1:p.Glu821Val
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ENST00000674773.1:c.1760A>T
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ENSP00000502579.1:p.Glu587Val
|
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ENST00000675517.1:c.2052A>T
|
|
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ENST00000676076.1:c.2038A>T
|
|
|
ENST00000676260.1:c.2139A>T
|
|
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ENST00000676316.1:c.2064A>T
|
|
|
ENST00000291825.11:c.*2382A>T
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ENSP00000291825.6:n.*2382A>T
|
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ENST00000324001.7:c.2177A>T
|
ENSP00000326018.6:p.Glu726Val
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NM_020956.2:c.*2382A>T , LRG_265t1:c.*2382A>T
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NP_066007.1:n.*2382A>T
|
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NM_181882.2:c.2177A>T , LRG_265t2:c.2177A>T
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NP_870998.2:p.Glu726Val
|
|
XM_011527171.1:c.2177A>T
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XP_011525473.1:p.Glu726Val
|
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XM_011527171.2:c.2177A>T
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XP_011525473.1:p.Glu726Val
|
|
XM_017027046.1:c.2075A>T
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XP_016882535.1:p.Glu692Val
|
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XM_017027047.1:c.2075A>T
|
XP_016882536.1:p.Glu692Val
|
|
NM_181882.3:c.2177A>T
MANE Select
|
NP_870998.2:p.Glu726Val
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