ENST00000336112.9:c.3945G=
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ENSP00000337250.5:p.Leu1315=
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ENST00000435504.9:c.3948G=
MANE Select
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ENSP00000391447.3:p.Leu1316=
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ENST00000336112.8:c.3864G=
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ENSP00000337250.4:p.Leu1288=
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ENST00000404843.5:c.2397G=
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ENSP00000383920.1:p.Leu799=
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ENST00000435504.8:c.3948G=
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ENSP00000391447.3:p.Leu1316=
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NM_018263.4:c.3948G=
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NP_060733.4:p.Leu1316=
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XM_006712039.2:c.3582G=
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XP_006712102.1:p.Leu1194=
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XM_006712040.1:c.3168G=
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XP_006712103.1:p.Leu1056=
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XM_011532950.1:c.3945G=
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XP_011531252.1:p.Leu1315=
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XM_011532951.1:c.3774G=
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XP_011531253.1:p.Leu1258=
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NM_018263.5:c.3948G=
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NP_060733.4:p.Leu1316=
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XM_006712039.3:c.3582G=
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XP_006712102.1:p.Leu1194=
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XM_006712040.2:c.3168G=
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XP_006712103.1:p.Leu1056=
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XM_011532950.3:c.3945G=
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XP_011531252.1:p.Leu1315=
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XM_011532951.2:c.3774G=
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XP_011531253.1:p.Leu1258=
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XM_017004430.1:c.3168G=
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XP_016859919.1:p.Leu1056=
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XM_024452974.1:c.4128G=
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XP_024308742.1:p.Leu1376=
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NM_001369346.1:c.3774G=
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NP_001356275.1:p.Leu1258=
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NM_001369347.1:c.3168G=
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NP_001356276.1:p.Leu1056=
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NM_018263.6:c.3948G=
MANE Select
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NP_060733.4:p.Leu1316=
|
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