ENST00000396705.10:c.693T>C
MANE Select
|
ENSP00000379933.4:p.Leu231=
|
|
ENST00000229270.8:c.804T>C
|
ENSP00000229270.4:p.Leu268=
|
|
ENST00000396705.9:c.693T>C
|
ENSP00000379933.4:p.Leu231=
|
|
ENST00000474253.1:n.182T>C
|
|
|
ENST00000488464.6:c.447T>C
|
ENSP00000475620.1:p.Leu149=
|
|
ENST00000535434.5:c.447T>C
|
ENSP00000443599.1:p.Leu149=
|
|
ENST00000613953.4:c.804T>C
|
ENSP00000484435.1:p.Leu268=
|
|
NM_000365.5:c.693T>C
|
NP_000356.1:p.Leu231=
|
|
NM_001159287.1:c.804T>C
|
NP_001152759.1:p.Leu268=
|
|
NM_001258026.1:c.447T>C
|
NP_001244955.1:p.Leu149=
|
|
XR_002957378.1:n.1701T>C
|
|
|
NM_000365.6:c.693T>C
MANE Select
|
NP_000356.1:p.Leu231=
|
|
NM_001258026.2:c.447T>C
|
NP_001244955.1:p.Leu149=
|
|