ENST00000324001.8:c.3423G>T
MANE Select
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ENSP00000326018.6:p.Ala1141=
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ENST00000673881.1:c.3006G>T
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ENSP00000501070.1:p.Ala1002=
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ENST00000674005.2:c.3708G>T
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ENSP00000501261.1:p.Ala1236=
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ENST00000674773.1:c.3006G>T
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ENSP00000502579.1:p.Ala1002=
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ENST00000675517.1:c.3298G>T
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ENST00000676076.1:c.3284G>T
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ENST00000676260.1:c.3385G>T
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ENST00000676316.1:c.3310G>T
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ENST00000291825.11:c.*3628G>T
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ENSP00000291825.6:n.*3628G>T
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ENST00000324001.7:c.3423G>T
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ENSP00000326018.6:p.Ala1141=
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NM_020956.2:c.*3628G>T , LRG_265t1:c.*3628G>T
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NP_066007.1:n.*3628G>T
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NM_181882.2:c.3423G>T , LRG_265t2:c.3423G>T
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NP_870998.2:p.Ala1141=
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XM_011527171.1:c.3423G>T
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XP_011525473.1:p.Ala1141=
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XM_011527171.2:c.3423G>T
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XP_011525473.1:p.Ala1141=
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XM_017027046.1:c.3321G>T
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XP_016882535.1:p.Ala1107=
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XM_017027047.1:c.3321G>T
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XP_016882536.1:p.Ala1107=
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NM_181882.3:c.3423G>T
MANE Select
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NP_870998.2:p.Ala1141=
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