|
ENST00000411732.4:c.653T>A
|
ENSP00000387634.1:p.Ile218Asn
|
|
|
ENST00000439032.6:c.1343T>A
|
ENSP00000509775.1:n.1343T>A
|
|
|
ENST00000637191.2:c.803T>A
|
ENSP00000490154.2:p.Ile268Asn
|
|
|
ENST00000690143.1:c.*735T>A
|
ENSP00000510306.1:n.*735T>A
|
|
|
ENST00000691610.1:c.842T>A
|
ENSP00000509830.1:p.Ile281Asn
|
|
|
ENST00000242480.4:c.803T>A
MANE Select
|
ENSP00000242480.3:p.Ile268Asn
|
|
|
ENST00000411732.3:c.653T>A
|
ENSP00000387634.1:p.Ile218Asn
|
|
|
ENST00000639815.1:n.109-873T>A
|
|
|
|
ENST00000242480.3:c.803T>A
|
ENSP00000242480.3:p.Ile268Asn
|
|
|
ENST00000411732.2:c.653T>A
|
ENSP00000387634.1:p.Ile218Asn
|
|
|
ENST00000439032.4:c.803T>A
|
ENSP00000402040.1:p.Ile268Asn
|
|
|
NM_000399.3:c.803T>A , LRG_239t1:c.803T>A
|
NP_000390.2:p.Ile268Asn
|
|
|
NM_001136177.1:c.803T>A
|
NP_001129649.1:p.Ile268Asn
|
|
|
NM_001136178.1:c.803T>A
|
NP_001129650.1:p.Ile268Asn
|
|
|
NM_001136179.1:c.653T>A
|
NP_001129651.1:p.Ile218Asn
|
|
|
XM_011539427.1:c.842T>A
|
XP_011537729.1:p.Ile281Asn
|
|
|
XM_011539428.1:c.653T>A
|
XP_011537730.1:p.Ile218Asn
|
|
|
XM_011539429.1:c.653T>A
|
XP_011537731.1:p.Ile218Asn
|
|
|
NM_000399.4:c.803T>A
|
NP_000390.2:p.Ile268Asn
|
|
|
NM_001136177.2:c.803T>A
|
NP_001129649.1:p.Ile268Asn
|
|
|
NM_001136179.2:c.653T>A
|
NP_001129651.1:p.Ile218Asn
|
|
|
NM_001321037.1:c.653T>A
|
NP_001307966.1:p.Ile218Asn
|
|
|
NM_000399.5:c.803T>A
MANE Select
|
NP_000390.2:p.Ile268Asn
|
|
|
NM_001136177.3:c.803T>A
|
NP_001129649.1:p.Ile268Asn
|
|
|
NM_001136179.3:c.653T>A
|
NP_001129651.1:p.Ile218Asn
|
|
|
NM_001321037.2:c.653T>A
|
NP_001307966.1:p.Ile218Asn
|
|
|
NM_001136178.2:c.803T>A
|
NP_001129650.1:p.Ile268Asn
|
|
