ENST00000262367.10:c.6108C>A
MANE Select
|
ENSP00000262367.5:p.Pro2036=
|
|
ENST00000262367.9:c.6108C>A
|
ENSP00000262367.5:p.Pro2036=
|
|
ENST00000382070.7:c.5994C>A
|
ENSP00000371502.3:p.Pro1998=
|
|
NM_001079846.1:c.5994C>A
|
NP_001073315.1:p.Pro1998=
|
|
NM_004380.2:c.6108C>A
|
NP_004371.2:p.Pro2036=
|
|
XM_005255124.3:c.6063C>A
|
XP_005255181.1:p.Pro2021=
|
|
XM_005255125.3:c.5691C>A
|
XP_005255182.1:p.Pro1897=
|
|
XM_006720848.2:c.5847C>A
|
XP_006720911.1:p.Pro1949=
|
|
XM_011522380.1:c.6054C>A
|
XP_011520682.1:p.Pro2018=
|
|
XM_011522381.1:c.5355C>A
|
XP_011520683.1:p.Pro1785=
|
|
XM_005255124.4:c.6063C>A
|
XP_005255181.1:p.Pro2021=
|
|
XM_005255125.4:c.5691C>A
|
XP_005255182.1:p.Pro1897=
|
|
XM_006720848.3:c.5847C>A
|
XP_006720911.1:p.Pro1949=
|
|
XM_011522381.2:c.5355C>A
|
XP_011520683.1:p.Pro1785=
|
|
XM_017022944.1:c.6102C>A
|
XP_016878433.1:p.Pro2034=
|
|
NM_004380.3:c.6108C>A
MANE Select
|
NP_004371.2:p.Pro2036=
|
|