ENST00000370096.9:c.3224G>A
MANE Select
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ENSP00000359114.3:p.Gly1075Glu
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ENST00000353414.8:c.3107G>A
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ENSP00000302551.6:p.Gly1036Glu
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ENST00000358392.6:c.3260G>A
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ENSP00000351163.2:p.Gly1087Glu
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ENST00000370096.7:c.3224G>A
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ENSP00000359114.3:p.Gly1075Glu
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ENST00000512756.5:c.2876G>A
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ENSP00000426533.1:p.Gly959Glu
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ENST00000635193.1:c.2558G>A
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NM_001190709.1:c.3107G>A
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NP_001177638.1:p.Gly1036Glu
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NM_001854.3:c.3224G>A
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NP_001845.3:p.Gly1075Glu
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NM_080629.2:c.3260G>A
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NP_542196.2:p.Gly1087Glu
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NM_080630.3:c.2876G>A
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NP_542197.3:p.Gly959Glu
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XM_011540719.1:c.3224G>A
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XP_011539021.1:p.Gly1075Glu
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XM_011540720.1:c.1457G>A
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XP_011539022.1:p.Gly486Glu
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XM_011540721.1:c.812G>A
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XP_011539023.1:p.Gly271Glu
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NR_134980.1:n.3558G>A
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|
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XM_017000334.1:c.3377G>A
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XP_016855823.1:p.Gly1126Glu
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XM_017000335.1:c.3371G>A
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XP_016855824.1:p.Gly1124Glu
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XM_017000336.1:c.3377G>A
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XP_016855825.1:p.Gly1126Glu
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XM_017000337.1:c.1775G>A
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XP_016855826.1:p.Gly592Glu
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NM_001854.4:c.3224G>A
MANE Select
|
NP_001845.3:p.Gly1075Glu
|
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NM_080630.4:c.2876G>A
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NP_542197.3:p.Gly959Glu
|
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NR_134980.2:n.3584G>A
|
|
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NM_001190709.2:c.3107G>A
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NP_001177638.1:p.Gly1036Glu
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NM_080629.3:c.3260G>A
|
NP_542196.2:p.Gly1087Glu
|
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