ENST00000262367.10:c.7198T=
MANE Select
|
ENSP00000262367.5:p.Leu2400=
|
|
ENST00000262367.9:c.7198T=
|
ENSP00000262367.5:p.Leu2400=
|
|
ENST00000382070.7:c.7084T=
|
ENSP00000371502.3:p.Leu2362=
|
|
NM_001079846.1:c.7084T=
|
NP_001073315.1:p.Leu2362=
|
|
NM_004380.2:c.7198T=
|
NP_004371.2:p.Leu2400=
|
|
XM_005255124.3:c.7153T=
|
XP_005255181.1:p.Leu2385=
|
|
XM_005255125.3:c.6781T=
|
XP_005255182.1:p.Leu2261=
|
|
XM_006720848.2:c.6937T=
|
XP_006720911.1:p.Leu2313=
|
|
XM_011522380.1:c.7144T=
|
XP_011520682.1:p.Leu2382=
|
|
XM_011522381.1:c.6445T=
|
XP_011520683.1:p.Leu2149=
|
|
XM_005255124.4:c.7153T=
|
XP_005255181.1:p.Leu2385=
|
|
XM_005255125.4:c.6781T=
|
XP_005255182.1:p.Leu2261=
|
|
XM_006720848.3:c.6937T=
|
XP_006720911.1:p.Leu2313=
|
|
XM_011522381.2:c.6445T=
|
XP_011520683.1:p.Leu2149=
|
|
XM_017022944.1:c.7192T=
|
XP_016878433.1:p.Leu2398=
|
|
NM_004380.3:c.7198T=
MANE Select
|
NP_004371.2:p.Leu2400=
|
|