ENST00000394867.9:n.1480T>G
|
|
|
ENST00000688002.1:n.3192T>G
|
|
|
ENST00000688751.1:n.177T>G
|
|
|
ENST00000689792.1:n.945T>G
|
|
|
ENST00000262948.10:c.1041T>G
MANE Select
|
ENSP00000262948.4:p.Asn347Lys
|
|
ENST00000262948.9:c.1041T>G
|
ENSP00000262948.3:p.Asn347Lys
|
|
ENST00000394867.8:c.750T>G
|
ENSP00000378336.1:p.Asn250Lys
|
|
ENST00000595715.1:n.856T>G
|
|
|
ENST00000597263.5:n.226T>G
|
|
|
ENST00000599021.1:c.151T>G
|
|
|
ENST00000600584.5:n.1601T>G
|
|
|
ENST00000601786.5:n.1342T>G
|
|
|
NM_030662.3:c.1041T>G , LRG_750t1:c.1041T>G
|
NP_109587.1:p.Asn347Lys
|
|
XM_006722799.2:c.762T>G
|
XP_006722862.1:p.Asn254Lys
|
|
XM_011528133.1:c.471T>G
|
XP_011526435.1:p.Asn157Lys
|
|
XM_017026989.1:c.1041T>G
|
XP_016882478.1:p.Asn347Lys
|
|
XM_017026990.1:c.762T>G
|
XP_016882479.1:p.Asn254Lys
|
|
NM_030662.4:c.1041T>G
MANE Select
|
NP_109587.1:p.Asn347Lys
|
|