ENST00000261819.8:c.1839G>A
MANE Select
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ENSP00000261819.3:p.Glu613=
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ENST00000261819.7:c.1839G>A
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ENSP00000261819.3:p.Glu613=
|
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ENST00000441917.6:c.1503G>A
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ENSP00000415061.2:p.Glu501=
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ENST00000534976.5:n.2571G>A
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|
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ENST00000535482.1:c.837G>A
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ENSP00000438754.1:p.Glu279=
|
|
ENST00000535641.5:n.2050G>A
|
|
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ENST00000539079.5:c.1163G>A
|
|
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ENST00000541887.5:c.1800G>A
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ENSP00000439875.1:p.Glu600=
|
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ENST00000544314.5:n.957G>A
|
|
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ENST00000545218.5:n.1009G>A
|
|
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NM_001137559.1:c.1503G>A
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NP_001131031.1:p.Glu501=
|
|
NM_016237.4:c.1839G>A
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NP_057321.2:p.Glu613=
|
|
XM_005253900.2:c.1800G>A
|
XP_005253957.1:p.Glu600=
|
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XM_006719449.1:c.645G>A
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XP_006719512.1:p.Glu215=
|
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NM_001330489.1:c.1800G>A
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NP_001317418.1:p.Glu600=
|
|
XM_017019423.2:c.645G>A
|
XP_016874912.1:p.Glu215=
|
|
XM_017019424.2:c.645G>A
|
XP_016874913.1:p.Glu215=
|
|
NM_016237.5:c.1839G>A
MANE Select
|
NP_057321.2:p.Glu613=
|
|
NM_001330489.2:c.1800G>A
|
NP_001317418.1:p.Glu600=
|
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