ENST00000370096.9:c.3884C>G
MANE Select
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ENSP00000359114.3:p.Ala1295Gly
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ENST00000353414.8:c.3767C>G
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ENSP00000302551.6:p.Ala1256Gly
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ENST00000358392.6:c.3920C>G
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ENSP00000351163.2:p.Ala1307Gly
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ENST00000370096.7:c.3884C>G
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ENSP00000359114.3:p.Ala1295Gly
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ENST00000512756.5:c.3536C>G
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ENSP00000426533.1:p.Ala1179Gly
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ENST00000635193.1:c.3218C>G
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NM_001190709.1:c.3767C>G
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NP_001177638.1:p.Ala1256Gly
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NM_001854.3:c.3884C>G
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NP_001845.3:p.Ala1295Gly
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NM_080629.2:c.3920C>G
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NP_542196.2:p.Ala1307Gly
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NM_080630.3:c.3536C>G
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NP_542197.3:p.Ala1179Gly
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XM_011540719.1:c.3884C>G
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XP_011539021.1:p.Ala1295Gly
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XM_011540720.1:c.2117C>G
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XP_011539022.1:p.Ala706Gly
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XM_011540721.1:c.1472C>G
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XP_011539023.1:p.Ala491Gly
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NR_134980.1:n.4218C>G
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XM_017000334.1:c.4037C>G
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XP_016855823.1:p.Ala1346Gly
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XM_017000335.1:c.4031C>G
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XP_016855824.1:p.Ala1344Gly
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XM_017000336.1:c.4037C>G
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XP_016855825.1:p.Ala1346Gly
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XM_017000337.1:c.2435C>G
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XP_016855826.1:p.Ala812Gly
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NM_001854.4:c.3884C>G
MANE Select
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NP_001845.3:p.Ala1295Gly
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NM_080630.4:c.3536C>G
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NP_542197.3:p.Ala1179Gly
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NR_134980.2:n.4244C>G
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NM_001190709.2:c.3767C>G
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NP_001177638.1:p.Ala1256Gly
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NM_080629.3:c.3920C>G
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NP_542196.2:p.Ala1307Gly
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