ENST00000322776.11:c.651G>T
MANE Select
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ENSP00000322450.6:p.Glu217Asp
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ENST00000647561.1:c.651G>T
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ENSP00000497587.1:p.Glu217Asp
|
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ENST00000322776.10:c.651G>T
|
ENSP00000322450.6:p.Glu217Asp
|
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ENST00000415352.6:c.630G>T
|
ENSP00000395368.2:p.Glu210Asp
|
|
ENST00000526169.1:n.393G>T
|
|
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ENST00000526770.5:n.510G>T
|
|
|
ENST00000529927.5:c.624G>T
|
ENSP00000436766.1:p.Glu208Asp
|
|
ENST00000532244.5:c.348G>T
|
ENSP00000435202.1:p.Glu116Asp
|
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ENST00000532303.5:c.348G>T
|
ENSP00000432015.1:p.Glu116Asp
|
|
ENST00000533919.5:c.129G>T
|
ENSP00000435199.1:p.Glu43Asp
|
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NM_001166102.1:c.624G>T
|
NP_001159574.1:p.Glu208Asp
|
|
NM_007103.3:c.651G>T
|
NP_009034.2:p.Glu217Asp
|
|
NM_001166102.2:c.624G>T
|
NP_001159574.1:p.Glu208Asp
|
|
NM_007103.4:c.651G>T
MANE Select
|
NP_009034.2:p.Glu217Asp
|
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