ENST00000347401.8:c.227G>C
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|
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ENST00000353578.9:c.6964G>C
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ENSP00000315873.4:p.Glu2322Gln
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ENST00000295550.9:c.7582G>C
MANE Select
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ENSP00000295550.4:p.Glu2528Gln
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ENST00000295550.8:c.7582G>C
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ENSP00000295550.4:p.Glu2528Gln
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ENST00000347401.7:c.5758G>C
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ENSP00000315609.4:p.Glu1920Gln
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ENST00000353578.8:c.6964G>C
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ENSP00000315873.4:p.Glu2322Gln
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ENST00000409809.5:c.6964G>C
|
ENSP00000386844.1:p.Glu2322Gln
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ENST00000472056.5:c.5761G>C
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ENSP00000418285.1:p.Glu1921Gln
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ENST00000491769.1:n.1836G>C
|
|
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NM_004369.3:c.7582G>C , LRG_473t1:c.7582G>C
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NP_004360.2:p.Glu2528Gln
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NM_057166.4:c.5761G>C
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NP_476507.3:p.Glu1921Gln
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NM_057167.3:c.6964G>C
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NP_476508.2:p.Glu2322Gln
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|
XM_005246065.1:c.6982G>C
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XP_005246122.1:p.Glu2328Gln
|
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XM_005246066.1:c.6361G>C
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XP_005246123.1:p.Glu2121Gln
|
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XM_006712253.1:c.7081G>C
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XP_006712316.1:p.Glu2361Gln
|
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XM_011510574.1:c.7579G>C
|
XP_011508876.1:p.Glu2527Gln
|
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XM_011510575.1:c.5176G>C
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XP_011508877.1:p.Glu1726Gln
|
|
XM_017003304.1:c.5176G>C
|
XP_016858793.1:p.Glu1726Gln
|
|
XM_024452684.1:c.6361G>C
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XP_024308452.1:p.Glu2121Gln
|
|
NM_004369.4:c.7582G>C
MANE Select
|
NP_004360.2:p.Glu2528Gln
|
|
NM_057166.5:c.5761G>C
|
NP_476507.3:p.Glu1921Gln
|
|
NM_057167.4:c.6964G>C
|
NP_476508.2:p.Glu2322Gln
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