ENST00000262493.12:c.819T>C
MANE Select
|
ENSP00000262493.6:p.Asp273=
|
|
ENST00000562316.6:c.486T>C
|
ENSP00000457238.2:p.Asp162=
|
|
ENST00000564727.2:c.123T>C
|
ENSP00000454971.2:p.Asp41=
|
|
ENST00000568375.2:c.116-3387T>C
|
|
|
ENST00000638185.1:n.1034T>C
|
|
|
ENST00000638210.1:n.1119T>C
|
|
|
ENST00000638705.1:c.819T>C
|
ENSP00000491223.1:p.Asp273=
|
|
ENST00000638836.1:n.729T>C
|
|
|
ENST00000639055.1:n.1540T>C
|
|
|
ENST00000639251.1:n.720T>C
|
|
|
ENST00000639268.1:c.454T>C
|
|
|
ENST00000639341.1:c.344T>C
|
|
|
ENST00000639770.1:c.857T>C
|
ENSP00000491999.1:n.857T>C
|
|
ENST00000640390.1:n.749T>C
|
|
|
ENST00000640469.1:c.183T>C
|
ENSP00000491875.1:p.Asp61=
|
|
ENST00000640560.1:n.595T>C
|
|
|
ENST00000640893.1:c.*217T>C
|
ENSP00000492677.1:n.*217T>C
|
|
ENST00000262493.10:c.819T>C
|
ENSP00000262493.6:p.Asp273=
|
|
ENST00000564727.1:c.39T>C
|
ENSP00000454971.1:p.Asp13=
|
|
ENST00000568375.1:n.116-3387T>C
|
|
|
NM_020988.2:c.819T>C
|
NP_066268.1:p.Asp273=
|
|
XM_011523003.1:c.693T>C
|
XP_011521305.1:p.Asp231=
|
|
XM_011523003.3:c.693T>C
|
XP_011521305.1:p.Asp231=
|
|
NM_020988.3:c.819T>C
MANE Select
|
NP_066268.1:p.Asp273=
|
|