ENST00000262367.10:c.6261G>C
MANE Select
|
ENSP00000262367.5:p.Leu2087=
|
|
ENST00000262367.9:c.6261G>C
|
ENSP00000262367.5:p.Leu2087=
|
|
ENST00000382070.7:c.6147G>C
|
ENSP00000371502.3:p.Leu2049=
|
|
NM_001079846.1:c.6147G>C
|
NP_001073315.1:p.Leu2049=
|
|
NM_004380.2:c.6261G>C
|
NP_004371.2:p.Leu2087=
|
|
XM_005255124.3:c.6216G>C
|
XP_005255181.1:p.Leu2072=
|
|
XM_005255125.3:c.5844G>C
|
XP_005255182.1:p.Leu1948=
|
|
XM_006720848.2:c.6000G>C
|
XP_006720911.1:p.Leu2000=
|
|
XM_011522380.1:c.6207G>C
|
XP_011520682.1:p.Leu2069=
|
|
XM_011522381.1:c.5508G>C
|
XP_011520683.1:p.Leu1836=
|
|
XM_005255124.4:c.6216G>C
|
XP_005255181.1:p.Leu2072=
|
|
XM_005255125.4:c.5844G>C
|
XP_005255182.1:p.Leu1948=
|
|
XM_006720848.3:c.6000G>C
|
XP_006720911.1:p.Leu2000=
|
|
XM_011522381.2:c.5508G>C
|
XP_011520683.1:p.Leu1836=
|
|
XM_017022944.1:c.6255G>C
|
XP_016878433.1:p.Leu2085=
|
|
NM_004380.3:c.6261G>C
MANE Select
|
NP_004371.2:p.Leu2087=
|
|