ENST00000456935.7:c.1224C=
MANE Select
|
ENSP00000395473.2:p.Phe408=
|
|
ENST00000221363.8:c.1221C=
|
ENSP00000221363.4:p.Phe407=
|
|
ENST00000456935.6:c.1224C=
|
ENSP00000395473.2:p.Phe408=
|
|
ENST00000465830.1:n.388C=
|
|
|
ENST00000466794.5:n.1123C=
|
|
|
ENST00000495617.1:n.281-470C=
|
|
|
NM_000528.3:c.1224C=
|
NP_000519.2:p.Phe408=
|
|
NM_001173498.1:c.1221C=
|
NP_001166969.1:p.Phe407=
|
|
XM_005259913.1:c.1227C=
|
XP_005259970.1:p.Phe409=
|
|
XM_011528017.1:c.123C=
|
XP_011526319.1:p.Phe41=
|
|
XM_005259913.2:c.1227C=
|
XP_005259970.1:p.Phe409=
|
|
XM_024451518.1:c.123C=
|
XP_024307286.1:p.Phe41=
|
|
NM_000528.4:c.1224C=
MANE Select
|
NP_000519.2:p.Phe408=
|
|
NM_001173498.2:c.1221C=
|
NP_001166969.1:p.Phe407=
|
|