ENST00000382103.7:c.954T>G
MANE Select
|
ENSP00000371535.2:p.Pro318=
|
|
ENST00000680581.1:c.954T>G
|
ENSP00000506483.1:p.Pro318=
|
|
ENST00000680824.1:n.2170T>G
|
|
|
ENST00000681071.1:n.1246T>G
|
|
|
ENST00000681341.1:n.2095T>G
|
|
|
ENST00000681948.1:c.1209T>G
|
ENSP00000505991.1:p.Pro403=
|
|
ENST00000358971.7:c.*752T>G
|
ENSP00000351857.3:n.*752T>G
|
|
ENST00000382103.6:c.954T>G
|
ENSP00000371535.2:p.Pro318=
|
|
ENST00000503150.1:c.236T>G
|
|
|
ENST00000505513.1:n.254T>G
|
|
|
ENST00000514585.5:c.*655T>G
|
ENSP00000421880.1:n.*655T>G
|
|
NM_016955.3:c.954T>G
|
NP_058651.3:p.Pro318=
|
|
XM_005248168.2:c.717T>G
|
XP_005248225.1:p.Pro239=
|
|
XM_006713965.2:c.774T>G
|
XP_006714028.1:p.Pro258=
|
|
XM_011513846.1:c.951T>G
|
XP_011512148.1:p.Pro317=
|
|
XM_011513847.1:c.921T>G
|
XP_011512149.1:p.Pro307=
|
|
XM_011513848.1:c.774T>G
|
XP_011512150.1:p.Pro258=
|
|
XM_011513846.2:c.951T>G
|
XP_011512148.1:p.Pro317=
|
|
XM_011513847.2:c.921T>G
|
XP_011512149.1:p.Pro307=
|
|
XM_017008277.1:c.1209T>G
|
XP_016863766.1:p.Pro403=
|
|
XM_017008278.1:c.531T>G
|
XP_016863767.1:p.Pro177=
|
|
NM_016955.4:c.954T>G
MANE Select
|
NP_058651.3:p.Pro318=
|
|