ENST00000297056.11:c.393C>T
MANE Select
|
ENSP00000297056.6:p.Asn131=
|
|
ENST00000297056.10:c.393C>T
|
ENSP00000297056.6:p.Asn131=
|
|
ENST00000425398.6:c.393C>T
|
ENSP00000391171.2:p.Asn131=
|
|
ENST00000432248.1:c.393C>T
|
ENSP00000410787.1:p.Asn131=
|
|
ENST00000436575.5:c.270C>T
|
ENSP00000404785.1:p.Asn90=
|
|
ENST00000454738.5:c.248-3429C>T
|
ENSP00000411746.1:n.248-3429C>T
|
|
ENST00000479922.6:n.483C>T
|
|
|
NM_001142936.1:c.393C>T
|
NP_001136408.1:p.Asn131=
|
|
NM_139179.3:c.393C>T
|
NP_631918.3:p.Asn131=
|
|
NM_139179.4:c.393C>T
MANE Select
|
NP_631918.3:p.Asn131=
|
|
NM_001142936.2:c.393C>T
|
NP_001136408.1:p.Asn131=
|
|