ENST00000348974.5:c.1668T>G
|
ENSP00000330021.7:p.Asn556Lys
|
|
ENST00000394236.9:c.1668T>G
MANE Select
|
ENSP00000377783.3:p.Asn556Lys
|
|
ENST00000407433.6:c.1623T>G
|
ENSP00000385794.2:p.Asn541Lys
|
|
ENST00000647936.1:c.1644+1995T>G
|
ENSP00000496822.1:n.1644+1995T>G
|
|
ENST00000648381.1:n.1836T>G
|
|
|
ENST00000648853.1:c.1626T>G
|
ENSP00000497262.1:p.Asn542Lys
|
|
ENST00000649103.1:c.1767T>G
|
ENSP00000497962.1:n.1767T>G
|
|
ENST00000649585.1:c.611T>G
|
ENSP00000498163.1:n.611T>G
|
|
ENST00000650591.1:c.1764T>G
|
ENSP00000497376.1:p.Asn588Lys
|
|
ENST00000394236.7:c.1668T>G
|
ENSP00000377783.3:p.Asn556Lys
|
|
ENST00000407433.5:c.1275T>G
|
ENSP00000385794.1:p.Asn425Lys
|
|
NM_000313.3:c.1668T>G , LRG_572t1:c.1668T>G
|
NP_000304.2:p.Asn556Lys
|
|
NM_001314077.1:c.1764T>G , LRG_572t2:c.1764T>G
|
NP_001301006.1:p.Asn588Lys
|
|
NM_000313.4:c.1668T>G
MANE Select
|
NP_000304.2:p.Asn556Lys
|
|
NM_001314077.2:c.1764T>G
|
NP_001301006.1:p.Asn588Lys
|
|