ENST00000644991.3:c.1353T>C
MANE Select
|
ENSP00000495607.1:p.Asn451=
|
|
ENST00000614701.4:c.1353T>C
|
ENSP00000482885.1:p.Asn451=
|
|
ENST00000616559.4:c.1479T>C
|
ENSP00000483259.1:p.Asn493=
|
|
NM_001145026.1:c.1353T>C
|
NP_001138498.1:p.Asn451=
|
|
XM_011538290.1:c.1353T>C
|
XP_011536592.1:p.Asn451=
|
|
XM_017019273.1:c.2019T>C
|
XP_016874762.1:p.Asn673=
|
|
XM_017019274.1:c.2019T>C
|
XP_016874763.1:p.Asn673=
|
|
XM_017019275.1:c.2019T>C
|
XP_016874764.1:p.Asn673=
|
|
XR_001748688.1:n.2156T>C
|
|
|
XR_001748689.1:n.2156T>C
|
|
|
NM_001145026.2:c.1353T>C
MANE Select
|
NP_001138498.1:p.Asn451=
|
|