ENST00000348729.8:c.894T>G
MANE Select
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ENSP00000302701.4:p.Ala298=
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ENST00000348729.7:c.894T>G
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ENSP00000302701.4:p.Ala298=
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ENST00000353963.7:c.906T>G
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ENSP00000302851.5:p.Ala302=
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ENST00000504513.1:c.164+247T>G
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ENST00000506512.1:n.505T>G
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NM_005847.4:c.894T>G
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NP_005838.3:p.Ala298=
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NM_152685.3:c.906T>G
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NP_689898.2:p.Ala302=
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XM_005272148.3:c.1014T>G
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XP_005272205.3:p.Ala338=
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XM_005272149.3:c.1002T>G
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XP_005272206.3:p.Ala334=
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XM_006714741.2:c.1014T>G
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XP_006714804.2:p.Ala338=
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XM_011543765.1:c.1014T>G
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XP_011542067.1:p.Ala338=
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XM_011543766.1:c.795T>G
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XP_011542068.1:p.Ala265=
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XM_011543767.1:c.699T>G
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XP_011542069.1:p.Ala233=
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XM_011543768.1:c.579T>G
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XP_011542070.1:p.Ala193=
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XM_011543769.1:c.189T>G
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XP_011542071.1:p.Ala63=
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XM_005272149.4:c.1002T>G
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XP_005272206.3:p.Ala334=
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XM_011543765.2:c.1014T>G
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XP_011542067.1:p.Ala338=
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NM_005847.5:c.894T>G
MANE Select
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NP_005838.3:p.Ala298=
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NM_152685.4:c.906T>G
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NP_689898.2:p.Ala302=
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