ENST00000527701.6:c.*1308A>C
|
ENSP00000435718.2:n.*1308A>C
|
|
ENST00000533313.6:c.*1262A>C
|
ENSP00000431843.2:n.*1262A>C
|
|
ENST00000616349.5:c.1336A>C
MANE Select
|
ENSP00000479524.2:p.Asn446His
|
|
ENST00000332271.9:c.1336A>C
|
ENSP00000330031.5:p.Asn446His
|
|
ENST00000527701.5:c.1009A>C
|
ENSP00000435718.1:p.Asn337His
|
|
ENST00000532537.2:n.1757A>C
|
|
|
ENST00000533313.5:c.1009A>C
|
ENSP00000431843.1:p.Asn337His
|
|
ENST00000616349.4:c.1336A>C
|
ENSP00000479524.1:p.Asn446His
|
|
NM_001008496.3:c.1336A>C
|
NP_001008496.2:p.Asn446His
|
|
NM_001255975.1:c.1336A>C
MANE Select
|
NP_001242904.1:p.Asn446His
|
|
NR_045648.1:n.1967A>C
|
|
|
NR_045649.1:n.1840A>C
|
|
|
NR_045649.2:n.1840A>C
|
|
|