|
NM_173500.4:c.3466C>T
MANE Select
|
NP_775771.3:p.Arg1156Ter
|
|
ENST00000267890.11:c.3466C>T
MANE Select
|
ENSP00000267890.6:p.Arg1156Ter
|
|
NM_173500.3:c.3466C>T
|
NP_775771.3:p.Arg1156Ter
|
|
ENST00000267890.10:c.3466C>T
|
ENSP00000267890.6:p.Arg1156Ter
|
|
ENST00000622375.4:c.4681C>T
|
ENSP00000479984.1:p.Arg1561Ter
|
|
XM_005254171.3:c.3484C>T
|
XP_005254228.1:p.Arg1162Ter
|
|
XM_005254171.5:c.3484C>T
|
XP_005254228.1:p.Arg1162Ter
|
|
XM_005254173.3:c.3259C>T
|
XP_005254230.1:p.Arg1087Ter
|
|
XM_005254173.5:c.3259C>T
|
XP_005254230.1:p.Arg1087Ter
|
|
XM_006720402.2:c.3451C>T
|
XP_006720465.1:p.Arg1151Ter
|
|
XM_006720402.4:c.3451C>T
|
XP_006720465.1:p.Arg1151Ter
|
|
XM_006720403.2:c.3259C>T
|
XP_006720466.1:p.Arg1087Ter
|
|
XM_006720403.4:c.3259C>T
|
XP_006720466.1:p.Arg1087Ter
|
|
XM_011521267.1:c.3259C>T
|
XP_011519569.1:p.Arg1087Ter
|
|
XM_011521268.1:c.3199C>T
|
XP_011519570.1:p.Arg1067Ter
|
|
XM_011521269.1:c.3187C>T
|
XP_011519571.1:p.Arg1063Ter
|
|
XM_017021950.2:c.3187C>T
|
XP_016877439.1:p.Arg1063Ter
|
|
XM_024449849.1:c.3466C>T
|
XP_024305617.1:p.Arg1156Ter
|
|
XM_024449850.1:c.3466C>T
|
XP_024305618.1:p.Arg1156Ter
|
|
XM_024449851.1:c.3259C>T
|
XP_024305619.1:p.Arg1087Ter
|