ENST00000340855.11:c.896G>T
MANE Select
|
ENSP00000339801.6:p.Ser299Ile
|
|
ENST00000651111.1:c.263G>T
|
ENSP00000498395.1:p.Ser88Ile
|
|
ENST00000340855.10:c.896G>T
|
ENSP00000339801.6:p.Ser299Ile
|
|
ENST00000370441.8:c.896G>T
|
ENSP00000359470.4:p.Ser299Ile
|
|
ENST00000422081.6:c.263G>T
|
ENSP00000477056.1:p.Ser88Ile
|
|
ENST00000441880.1:n.114-3326G>T
|
|
|
ENST00000464251.5:c.822G>T
|
ENSP00000428980.1:n.822G>T
|
|
ENST00000466323.5:c.*87G>T
|
ENSP00000418264.1:n.*87G>T
|
|
ENST00000490775.5:n.681G>T
|
|
|
NM_000202.6:c.896G>T
|
NP_000193.1:p.Ser299Ile
|
|
NM_001166550.2:c.626G>T
|
NP_001160022.1:p.Ser209Ile
|
|
NM_006123.4:c.896G>T
|
NP_006114.1:p.Ser299Ile
|
|
NR_104128.1:n.1243G>T
|
|
|
NM_000202.7:c.896G>T
|
NP_000193.1:p.Ser299Ile
|
|
NM_001166550.3:c.626G>T
|
NP_001160022.1:p.Ser209Ile
|
|
NM_000202.8:c.896G>T
MANE Select
|
NP_000193.1:p.Ser299Ile
|
|
NM_001166550.4:c.626G>T
|
NP_001160022.1:p.Ser209Ile
|
|
NM_006123.5:c.896G>T
|
NP_006114.1:p.Ser299Ile
|
|
NR_104128.2:n.1195G>T
|
|
|