ENST00000370096.9:c.2350G>T
MANE Select
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ENSP00000359114.3:p.Gly784Cys
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ENST00000353414.8:c.2233G>T
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ENSP00000302551.6:p.Gly745Cys
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ENST00000358392.6:c.2386G>T
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ENSP00000351163.2:p.Gly796Cys
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ENST00000370096.7:c.2350G>T
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ENSP00000359114.3:p.Gly784Cys
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ENST00000512756.5:c.2002G>T
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ENSP00000426533.1:p.Gly668Cys
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ENST00000635193.1:c.1668G>T
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NM_001190709.1:c.2233G>T
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NP_001177638.1:p.Gly745Cys
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NM_001854.3:c.2350G>T
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NP_001845.3:p.Gly784Cys
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NM_080629.2:c.2386G>T
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NP_542196.2:p.Gly796Cys
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NM_080630.3:c.2002G>T
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NP_542197.3:p.Gly668Cys
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XM_011540719.1:c.2350G>T
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XP_011539021.1:p.Gly784Cys
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XM_011540720.1:c.583G>T
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XP_011539022.1:p.Gly195Cys
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XM_011540721.1:c.-79G>T
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XP_011539023.1:n.-79G>T
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XR_946545.1:n.2748G>T
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NR_134980.1:n.2668G>T
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XM_017000334.1:c.2503G>T
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XP_016855823.1:p.Gly835Cys
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XM_017000335.1:c.2497G>T
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XP_016855824.1:p.Gly833Cys
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XM_017000336.1:c.2503G>T
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XP_016855825.1:p.Gly835Cys
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XM_017000337.1:c.901G>T
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XP_016855826.1:p.Gly301Cys
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NM_001854.4:c.2350G>T
MANE Select
|
NP_001845.3:p.Gly784Cys
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NM_080630.4:c.2002G>T
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NP_542197.3:p.Gly668Cys
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NR_134980.2:n.2694G>T
|
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NM_001190709.2:c.2233G>T
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NP_001177638.1:p.Gly745Cys
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NM_080629.3:c.2386G>T
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NP_542196.2:p.Gly796Cys
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