ENST00000262367.10:c.7038A>G
MANE Select
|
ENSP00000262367.5:p.Pro2346=
|
|
ENST00000262367.9:c.7038A>G
|
ENSP00000262367.5:p.Pro2346=
|
|
ENST00000382070.7:c.6924A>G
|
ENSP00000371502.3:p.Pro2308=
|
|
NM_001079846.1:c.6924A>G
|
NP_001073315.1:p.Pro2308=
|
|
NM_004380.2:c.7038A>G
|
NP_004371.2:p.Pro2346=
|
|
XM_005255124.3:c.6993A>G
|
XP_005255181.1:p.Pro2331=
|
|
XM_005255125.3:c.6621A>G
|
XP_005255182.1:p.Pro2207=
|
|
XM_006720848.2:c.6777A>G
|
XP_006720911.1:p.Pro2259=
|
|
XM_011522380.1:c.6984A>G
|
XP_011520682.1:p.Pro2328=
|
|
XM_011522381.1:c.6285A>G
|
XP_011520683.1:p.Pro2095=
|
|
XM_005255124.4:c.6993A>G
|
XP_005255181.1:p.Pro2331=
|
|
XM_005255125.4:c.6621A>G
|
XP_005255182.1:p.Pro2207=
|
|
XM_006720848.3:c.6777A>G
|
XP_006720911.1:p.Pro2259=
|
|
XM_011522381.2:c.6285A>G
|
XP_011520683.1:p.Pro2095=
|
|
XM_017022944.1:c.7032A>G
|
XP_016878433.1:p.Pro2344=
|
|
NM_004380.3:c.7038A>G
MANE Select
|
NP_004371.2:p.Pro2346=
|
|