ENST00000527701.6:c.*1313A>T
|
ENSP00000435718.2:n.*1313A>T
|
|
ENST00000533313.6:c.*1267A>T
|
ENSP00000431843.2:n.*1267A>T
|
|
ENST00000616349.5:c.1341A>T
MANE Select
|
ENSP00000479524.2:p.Lys447Asn
|
|
ENST00000332271.9:c.1341A>T
|
ENSP00000330031.5:p.Lys447Asn
|
|
ENST00000527701.5:c.1014A>T
|
ENSP00000435718.1:p.Lys338Asn
|
|
ENST00000532537.2:n.1762A>T
|
|
|
ENST00000533313.5:c.1014A>T
|
ENSP00000431843.1:p.Lys338Asn
|
|
ENST00000616349.4:c.1341A>T
|
ENSP00000479524.1:p.Lys447Asn
|
|
NM_001008496.3:c.1341A>T
|
NP_001008496.2:p.Lys447Asn
|
|
NM_001255975.1:c.1341A>T
MANE Select
|
NP_001242904.1:p.Lys447Asn
|
|
NR_045648.1:n.1972A>T
|
|
|
NR_045649.1:n.1845A>T
|
|
|
NR_045649.2:n.1845A>T
|
|
|