ENST00000354177.9:c.1425C>T
|
ENSP00000346109.5:p.Gly475=
|
|
ENST00000494537.2:c.1583C>T
|
ENSP00000508308.1:n.1583C>T
|
|
ENST00000361547.7:c.1596C>T
MANE Select
|
ENSP00000355141.2:p.Gly532=
|
|
ENST00000354177.8:c.1494C>T
|
ENSP00000346109.4:p.Gly498=
|
|
ENST00000361547.6:c.1596C>T
|
ENSP00000355141.2:p.Gly532=
|
|
ENST00000374315.1:c.1494C>T
|
ENSP00000363434.1:p.Gly498=
|
|
ENST00000494537.1:n.363C>T
|
|
|
ENST00000527604.1:c.117C>T
|
ENSP00000457066.1:p.Gly39=
|
|
ENST00000559265.1:n.255+2293C>T
|
|
|
ENST00000630065.2:c.24C>T
|
ENSP00000487549.1:p.Gly8=
|
|
NM_020451.2:c.1596C>T
|
NP_065184.2:p.Gly532=
|
|
NM_206926.1:c.1494C>T
|
NP_996809.1:p.Gly498=
|
|
NM_020451.3:c.1596C>T
MANE Select
|
NP_065184.2:p.Gly532=
|
|
NM_206926.2:c.1494C>T
|
NP_996809.1:p.Gly498=
|
|