ENST00000402696.9:c.823A>G
MANE Select
|
ENSP00000385834.3:p.Met275Val
|
|
ENST00000402696.7:c.823A>G
|
ENSP00000385834.3:p.Met275Val
|
|
ENST00000485977.1:c.188A>G
|
ENSP00000418716.1:p.Tyr63Cys
|
|
NM_001063.3:c.823A>G
|
NP_001054.1:p.Met275Val
|
|
XM_011513100.1:c.823A>G
|
XP_011511402.1:p.Met275Val
|
|
NM_001354703.1:c.691A>G
|
NP_001341632.1:p.Met231Val
|
|
NM_001354704.1:c.442A>G
|
NP_001341633.1:p.Met148Val
|
|
NM_001063.4:c.823A>G
MANE Select
|
NP_001054.2:p.Met275Val
|
|
NM_001354703.2:c.691A>G
|
NP_001341632.2:p.Met231Val
|
|
NM_001354704.2:c.442A>G
|
NP_001341633.2:p.Met148Val
|
|