ENST00000398752.11:c.867T>C
MANE Select
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ENSP00000381736.5:p.Ala289=
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ENST00000282050.6:c.867T>C
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ENSP00000282050.2:p.Ala289=
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ENST00000398752.10:c.867T>C
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ENSP00000381736.5:p.Ala289=
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ENST00000586523.1:n.1272T>C
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|
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ENST00000586592.5:c.*930T>C
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ENSP00000466275.3:n.*930T>C
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ENST00000590156.5:c.*763T>C
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ENSP00000466309.1:n.*763T>C
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ENST00000590665.5:c.801T>C
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ENSP00000467037.1:p.Ala267=
|
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ENST00000592364.5:c.227-361T>C
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ENSP00000468618.1:n.227-361T>C
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ENST00000593152.6:c.717T>C
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ENSP00000465477.2:p.Ala239=
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NM_001001935.2:c.717T>C
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NP_001001935.1:p.Ala239=
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NM_001001937.1:c.867T>C
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NP_001001937.1:p.Ala289=
|
|
NM_001257334.1:c.801T>C
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NP_001244263.1:p.Ala267=
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NM_001257335.1:c.717T>C
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NP_001244264.1:p.Ala239=
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NM_004046.5:c.867T>C
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NP_004037.1:p.Ala289=
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XM_011526018.1:c.717T>C
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XP_011524320.1:p.Ala239=
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XM_017025789.1:c.867T>C
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XP_016881278.1:p.Ala289=
|
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NM_004046.6:c.867T>C
MANE Select
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NP_004037.1:p.Ala289=
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NM_001001935.3:c.717T>C
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NP_001001935.1:p.Ala239=
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NM_001257334.2:c.801T>C
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NP_001244263.1:p.Ala267=
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NM_001001937.2:c.867T>C
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NP_001001937.1:p.Ala289=
|
|
NM_001257335.2:c.717T>C
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NP_001244264.1:p.Ala239=
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