ENST00000347401.8:c.990A>G
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ENST00000353578.9:c.7727A>G
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ENSP00000315873.4:p.Glu2576Gly
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ENST00000682957.1:c.348A>G
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ENST00000684508.1:n.612A>G
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ENST00000295550.9:c.8345A>G
MANE Select
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ENSP00000295550.4:p.Glu2782Gly
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ENST00000295550.8:c.8345A>G
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ENSP00000295550.4:p.Glu2782Gly
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ENST00000347401.7:c.6521A>G
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ENSP00000315609.4:p.Glu2174Gly
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ENST00000353578.8:c.7727A>G
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ENSP00000315873.4:p.Glu2576Gly
|
|
ENST00000409809.5:c.7727A>G
|
ENSP00000386844.1:p.Glu2576Gly
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|
ENST00000468792.1:n.32A>G
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|
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ENST00000472056.5:c.6524A>G
|
ENSP00000418285.1:p.Glu2175Gly
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ENST00000491769.1:n.4787A>G
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|
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NM_004369.3:c.8345A>G , LRG_473t1:c.8345A>G
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NP_004360.2:p.Glu2782Gly
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NM_057166.4:c.6524A>G
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NP_476507.3:p.Glu2175Gly
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NM_057167.3:c.7727A>G
|
NP_476508.2:p.Glu2576Gly
|
|
XM_005246065.1:c.7745A>G
|
XP_005246122.1:p.Glu2582Gly
|
|
XM_005246066.1:c.7124A>G
|
XP_005246123.1:p.Glu2375Gly
|
|
XM_006712253.1:c.7844A>G
|
XP_006712316.1:p.Glu2615Gly
|
|
XM_011510574.1:c.8342A>G
|
XP_011508876.1:p.Glu2781Gly
|
|
XM_011510575.1:c.5939A>G
|
XP_011508877.1:p.Glu1980Gly
|
|
XM_017003304.1:c.5939A>G
|
XP_016858793.1:p.Glu1980Gly
|
|
XM_024452684.1:c.7124A>G
|
XP_024308452.1:p.Glu2375Gly
|
|
NM_004369.4:c.8345A>G
MANE Select
|
NP_004360.2:p.Glu2782Gly
|
|
NM_057166.5:c.6524A>G
|
NP_476507.3:p.Glu2175Gly
|
|
NM_057167.4:c.7727A>G
|
NP_476508.2:p.Glu2576Gly
|
|