ENST00000360228.11:c.5351A>T
MANE Select
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ENSP00000353362.5:p.Glu1784Val
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ENST00000573710.7:c.5357A>T
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ENSP00000460092.3:p.Glu1786Val
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ENST00000573891.6:c.770A>T
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|
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ENST00000574822.6:n.575A>T
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|
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ENST00000585802.6:c.512A>T
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ENSP00000465598.2:p.Glu171Val
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ENST00000635727.1:c.5354A>T
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ENSP00000490001.1:p.Glu1785Val
|
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ENST00000635742.1:n.1340A>T
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|
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ENST00000635895.1:c.5354A>T
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ENSP00000490323.1:p.Glu1785Val
|
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ENST00000636012.1:c.5354A>T
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ENSP00000490223.1:p.Glu1785Val
|
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ENST00000636389.1:c.5354A>T
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ENSP00000489992.1:p.Glu1785Val
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ENST00000636473.1:c.446A>T
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ENSP00000490173.1:p.Glu149Val
|
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ENST00000636549.1:c.5360A>T
|
ENSP00000490578.1:p.Glu1787Val
|
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ENST00000637276.1:c.5354A>T
|
ENSP00000489777.1:p.Glu1785Val
|
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ENST00000637432.1:c.5369A>T
|
ENSP00000490617.1:p.Glu1790Val
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|
ENST00000637736.1:c.5213A>T
|
ENSP00000489861.1:p.Glu1738Val
|
|
ENST00000637769.1:c.5354A>T
|
ENSP00000489778.1:p.Glu1785Val
|
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ENST00000637777.1:c.545A>T
|
|
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ENST00000637809.1:n.744A>T
|
|
|
ENST00000637819.1:c.755A>T
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ENSP00000490686.1:p.Glu252Val
|
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ENST00000637832.1:n.345A>T
|
|
|
ENST00000637927.1:c.5357A>T
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ENSP00000489715.1:p.Glu1786Val
|
|
ENST00000638009.2:c.5354A>T
|
ENSP00000489913.1:p.Glu1785Val
|
|
ENST00000638029.1:c.5369A>T
|
ENSP00000489829.1:p.Glu1790Val
|
|
ENST00000664864.1:c.5555A>T
|
ENSP00000499449.1:p.Glu1852Val
|
|
ENST00000360228.9:c.5351A>T
|
ENSP00000353362.5:p.Glu1784Val
|
|
ENST00000573710.6:c.5354A>T
|
ENSP00000460092.2:p.Glu1785Val
|
|
ENST00000573891.5:c.770A>T
|
|
|
ENST00000574822.5:n.575A>T
|
|
|
ENST00000585802.5:c.1409A>T
|
ENSP00000465598.1:p.Glu470Val
|
|
ENST00000587525.5:c.812A>T
|
ENSP00000467729.1:p.Glu271Val
|
|
ENST00000614285.4:c.5369A>T
|
ENSP00000479983.1:p.Glu1790Val
|
|
NM_000068.3:c.5369A>T
|
NP_000059.3:p.Glu1790Val
|
|
NM_001127221.1:c.5354A>T , LRG_7t1:c.5354A>T
|
NP_001120693.1:p.Glu1785Val
|
|
NM_001127222.1:c.5351A>T
|
NP_001120694.1:p.Glu1784Val
|
|
NM_001174080.1:c.5360A>T
|
NP_001167551.1:p.Glu1787Val
|
|
NM_023035.2:c.5369A>T
|
NP_075461.2:p.Glu1790Val
|
|
NM_000068.4:c.5369A>T
|
NP_000059.3:p.Glu1790Val
|
|
NM_001127222.2:c.5351A>T
MANE Select
|
NP_001120694.1:p.Glu1784Val
|
|
NM_001174080.2:c.5360A>T
|
NP_001167551.1:p.Glu1787Val
|
|
NM_023035.3:c.5369A>T
|
NP_075461.2:p.Glu1790Val
|
|
NM_001127221.2:c.5354A>T
|
NP_001120693.1:p.Glu1785Val
|
|