ENST00000322776.11:c.352G>A
MANE Select
|
ENSP00000322450.6:p.Asp118Asn
|
|
ENST00000647561.1:c.352G>A
|
ENSP00000497587.1:p.Asp118Asn
|
|
ENST00000322776.10:c.352G>A
|
ENSP00000322450.6:p.Asp118Asn
|
|
ENST00000415352.6:c.331G>A
|
ENSP00000395368.2:p.Asp111Asn
|
|
ENST00000524838.5:n.409G>A
|
|
|
ENST00000525086.5:n.425G>A
|
|
|
ENST00000526169.1:n.94G>A
|
|
|
ENST00000526770.5:n.211G>A
|
|
|
ENST00000528314.1:c.49G>A
|
ENSP00000434581.1:p.Asp17Asn
|
|
ENST00000528377.1:n.523G>A
|
|
|
ENST00000529867.5:c.316G>A
|
ENSP00000434438.1:p.Asp106Asn
|
|
ENST00000529927.5:c.325G>A
|
ENSP00000436766.1:p.Asp109Asn
|
|
ENST00000530014.5:n.647G>A
|
|
|
ENST00000530103.5:c.*246G>A
|
ENSP00000434575.1:n.*246G>A
|
|
ENST00000530638.1:c.235G>A
|
ENSP00000436936.1:p.Asp79Asn
|
|
ENST00000532244.5:c.49G>A
|
ENSP00000435202.1:p.Asp17Asn
|
|
ENST00000532303.5:c.49G>A
|
ENSP00000432015.1:p.Asp17Asn
|
|
ENST00000532343.5:c.49G>A
|
ENSP00000431751.1:p.Asp17Asn
|
|
ENST00000533075.5:c.331G>A
|
ENSP00000437267.1:p.Asp111Asn
|
|
ENST00000534139.5:n.468G>A
|
|
|
NM_001166102.1:c.325G>A
|
NP_001159574.1:p.Asp109Asn
|
|
NM_007103.3:c.352G>A
|
NP_009034.2:p.Asp118Asn
|
|
NM_001166102.2:c.325G>A
|
NP_001159574.1:p.Asp109Asn
|
|
NM_007103.4:c.352G>A
MANE Select
|
NP_009034.2:p.Asp118Asn
|
|