ENST00000393716.8:c.96T>C
MANE Select
|
ENSP00000377319.3:p.Asp32=
|
|
ENST00000466380.6:c.96T>C
|
ENSP00000420297.2:p.Asp32=
|
|
ENST00000648112.1:c.*119T>C
|
ENSP00000497876.1:n.*119T>C
|
|
ENST00000337940.4:c.213T>C
|
ENSP00000336528.4:p.Asp71=
|
|
ENST00000393716.6:c.96T>C
|
ENSP00000377319.2:p.Asp32=
|
|
ENST00000466380.5:c.96T>C
|
ENSP00000420297.1:p.Asp32=
|
|
ENST00000474090.1:n.384T>C
|
|
|
NM_003889.3:c.96T>C
|
NP_003880.3:p.Asp32=
|
|
NM_022002.2:c.213T>C
|
NP_071285.1:p.Asp71=
|
|
NM_033013.2:c.96T>C
|
NP_148934.1:p.Asp32=
|
|
NM_003889.4:c.96T>C
MANE Select
|
NP_003880.3:p.Asp32=
|
|
NM_022002.3:c.213T>C
|
NP_071285.1:p.Asp71=
|
|
NM_033013.3:c.96T>C
|
NP_148934.1:p.Asp32=
|
|