ENST00000324001.8:c.1170A>G
MANE Select
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ENSP00000326018.6:p.Arg390=
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ENST00000673881.1:c.753A>G
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ENSP00000501070.1:p.Arg251=
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ENST00000674005.2:c.1455A>G
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ENSP00000501261.1:p.Arg485=
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ENST00000674773.1:c.753A>G
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ENSP00000502579.1:p.Arg251=
|
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ENST00000675517.1:c.1045A>G
|
|
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ENST00000676076.1:c.1031A>G
|
|
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ENST00000676260.1:c.1132A>G
|
|
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ENST00000676316.1:c.1057A>G
|
|
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ENST00000291825.11:c.*1375A>G
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ENSP00000291825.6:n.*1375A>G
|
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ENST00000324001.7:c.1170A>G
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ENSP00000326018.6:p.Arg390=
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NM_020956.2:c.*1375A>G , LRG_265t1:c.*1375A>G
|
NP_066007.1:n.*1375A>G
|
|
NM_181882.2:c.1170A>G , LRG_265t2:c.1170A>G
|
NP_870998.2:p.Arg390=
|
|
XM_011527171.1:c.1170A>G
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XP_011525473.1:p.Arg390=
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XM_011527171.2:c.1170A>G
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XP_011525473.1:p.Arg390=
|
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XM_017027046.1:c.1068A>G
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XP_016882535.1:p.Arg356=
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XM_017027047.1:c.1068A>G
|
XP_016882536.1:p.Arg356=
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NM_181882.3:c.1170A>G
MANE Select
|
NP_870998.2:p.Arg390=
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