ENST00000303941.4:c.2061C>T
MANE Select
|
ENSP00000306678.3:p.Ala687=
|
|
ENST00000303941.3:c.2061C>T
|
ENSP00000306678.3:p.Ala687=
|
|
NM_178510.1:c.2061C>T
|
NP_848605.1:p.Ala687=
|
|
XM_011542736.1:c.2094C>T
|
XP_011541038.1:p.Ala698=
|
|
XM_011542737.1:c.2064C>T
|
XP_011541039.1:p.Ala688=
|
|
XM_011542738.1:c.1872C>T
|
XP_011541040.1:p.Ala624=
|
|
XM_011542736.2:c.2094C>T
|
XP_011541038.1:p.Ala698=
|
|
XM_011542737.2:c.2064C>T
|
XP_011541039.1:p.Ala688=
|
|
XM_011542738.2:c.1872C>T
|
XP_011541040.1:p.Ala624=
|
|
XM_017017475.1:c.2091C>T
|
XP_016872964.1:p.Ala697=
|
|
NM_178510.2:c.2061C>T
MANE Select
|
NP_848605.1:p.Ala687=
|
|