ENST00000682114.1:c.572+15C>T
|
ENSP00000507245.1:n.572+15C>T
|
|
ENST00000682478.1:n.762+15C>T
|
|
|
ENST00000683576.1:n.777C>T
|
|
|
ENST00000683627.1:c.587C>T
|
ENSP00000507533.1:p.Ser196Phe
|
|
ENST00000684082.1:c.544C>T
|
ENSP00000508266.1:n.544C>T
|
|
ENST00000684633.1:n.559C>T
|
|
|
ENST00000684678.1:c.568+15C>T
|
ENSP00000507059.1:n.568+15C>T
|
|
ENST00000369842.9:c.587C>T
MANE Select
|
ENSP00000358857.4:p.Ser196Phe
|
|
ENST00000369835.3:c.482C>T
|
ENSP00000358850.3:p.Ser161Phe
|
|
ENST00000369842.8:c.587C>T
|
ENSP00000358857.4:p.Ser196Phe
|
|
ENST00000428228.5:c.*492C>T
|
ENSP00000401081.1:n.*492C>T
|
|
ENST00000471965.1:n.376C>T
|
|
|
ENST00000486738.5:n.1024C>T
|
|
|
ENST00000492448.1:n.570C>T
|
|
|
NM_000117.2:c.587C>T , LRG_745t1:c.587C>T
|
NP_000108.1:p.Ser196Phe
|
|
XM_024452349.1:c.593C>T
|
XP_024308117.1:p.Ser198Phe
|
|
NM_000117.3:c.587C>T
MANE Select
|
NP_000108.1:p.Ser196Phe
|
|