ENST00000324001.8:c.2269G>C
MANE Select
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ENSP00000326018.6:p.Glu757Gln
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ENST00000673881.1:c.1852G>C
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ENSP00000501070.1:p.Glu618Gln
|
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ENST00000674005.2:c.2554G>C
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ENSP00000501261.1:p.Glu852Gln
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ENST00000674773.1:c.1852G>C
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ENSP00000502579.1:p.Glu618Gln
|
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ENST00000675517.1:c.2144G>C
|
|
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ENST00000676076.1:c.2130G>C
|
|
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ENST00000676260.1:c.2231G>C
|
|
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ENST00000676316.1:c.2156G>C
|
|
|
ENST00000291825.11:c.*2474G>C
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ENSP00000291825.6:n.*2474G>C
|
|
ENST00000324001.7:c.2269G>C
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ENSP00000326018.6:p.Glu757Gln
|
|
NM_020956.2:c.*2474G>C , LRG_265t1:c.*2474G>C
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NP_066007.1:n.*2474G>C
|
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NM_181882.2:c.2269G>C , LRG_265t2:c.2269G>C
|
NP_870998.2:p.Glu757Gln
|
|
XM_011527171.1:c.2269G>C
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XP_011525473.1:p.Glu757Gln
|
|
XM_011527171.2:c.2269G>C
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XP_011525473.1:p.Glu757Gln
|
|
XM_017027046.1:c.2167G>C
|
XP_016882535.1:p.Glu723Gln
|
|
XM_017027047.1:c.2167G>C
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XP_016882536.1:p.Glu723Gln
|
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NM_181882.3:c.2269G>C
MANE Select
|
NP_870998.2:p.Glu757Gln
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|