ENST00000262367.10:c.6042C>A
MANE Select
|
ENSP00000262367.5:p.Pro2014=
|
|
ENST00000262367.9:c.6042C>A
|
ENSP00000262367.5:p.Pro2014=
|
|
ENST00000382070.7:c.5928C>A
|
ENSP00000371502.3:p.Pro1976=
|
|
NM_001079846.1:c.5928C>A
|
NP_001073315.1:p.Pro1976=
|
|
NM_004380.2:c.6042C>A
|
NP_004371.2:p.Pro2014=
|
|
XM_005255124.3:c.5997C>A
|
XP_005255181.1:p.Pro1999=
|
|
XM_005255125.3:c.5625C>A
|
XP_005255182.1:p.Pro1875=
|
|
XM_006720848.2:c.5781C>A
|
XP_006720911.1:p.Pro1927=
|
|
XM_011522380.1:c.5988C>A
|
XP_011520682.1:p.Pro1996=
|
|
XM_011522381.1:c.5289C>A
|
XP_011520683.1:p.Pro1763=
|
|
XM_005255124.4:c.5997C>A
|
XP_005255181.1:p.Pro1999=
|
|
XM_005255125.4:c.5625C>A
|
XP_005255182.1:p.Pro1875=
|
|
XM_006720848.3:c.5781C>A
|
XP_006720911.1:p.Pro1927=
|
|
XM_011522381.2:c.5289C>A
|
XP_011520683.1:p.Pro1763=
|
|
XM_017022944.1:c.6036C>A
|
XP_016878433.1:p.Pro2012=
|
|
NM_004380.3:c.6042C>A
MANE Select
|
NP_004371.2:p.Pro2014=
|
|