ENST00000375190.10:c.*67C>G
MANE Select
|
ENSP00000364336.4:n.*67C>G
|
|
ENST00000375190.8:c.*67C>G
|
ENSP00000364336.3:n.*67C>G
|
|
ENST00000411851.3:c.983+116C>G
|
ENSP00000393333.2:n.983+116C>G
|
|
ENST00000589966.1:c.710C>G
|
ENSP00000468145.1:p.Ala237Gly
|
|
NM_001060.5:c.*67C>G , LRG_578t1:c.*67C>G
|
NP_001051.1:n.*67C>G
|
|
NM_201636.2:c.983+116C>G
|
NP_963998.2:n.983+116C>G
|
|
XM_011528214.1:c.*67C>G
|
XP_011526516.1:n.*67C>G
|
|
XM_011528214.2:c.*67C>G
|
XP_011526516.1:n.*67C>G
|
|
NM_001060.6:c.*67C>G
MANE Select
|
NP_001051.1:n.*67C>G
|
|
NM_201636.3:c.983+116C>G
|
NP_963998.2:n.983+116C>G
|
|