ENST00000348931.9:c.567C>T
MANE Select
|
ENSP00000335384.5:p.Cys189=
|
|
ENST00000348931.8:c.567C>T
|
ENSP00000335384.5:p.Cys189=
|
|
ENST00000377940.3:c.501C>T
|
ENSP00000367174.3:p.Cys167=
|
|
ENST00000583811.5:c.213C>T
|
ENSP00000462463.1:p.Cys71=
|
|
ENST00000584588.5:c.407-614C>T
|
ENSP00000462067.1:n.407-614C>T
|
|
NM_198844.2:c.501C>T
|
NP_942141.2:p.Cys167=
|
|
NM_199321.2:c.567C>T
|
NP_955353.1:p.Cys189=
|
|
XM_011524298.1:c.567C>T
|
XP_011522600.1:p.Cys189=
|
|
XR_002957959.1:n.758C>T
|
|
|
NM_198844.3:c.501C>T
|
NP_942141.2:p.Cys167=
|
|
NM_199321.3:c.567C>T
MANE Select
|
NP_955353.1:p.Cys189=
|
|