ENST00000703162.1:n.231C>G
|
|
|
ENST00000281043.4:c.882C>G
MANE Select
|
ENSP00000281043.3:p.Val294=
|
|
ENST00000638417.1:c.249C>G
|
ENSP00000491476.1:p.Val83=
|
|
ENST00000281043.3:c.882C>G
|
ENSP00000281043.3:p.Val294=
|
|
NM_001293228.1:c.882C>G
|
NP_001280157.1:p.Val294=
|
|
NM_001293231.1:c.249C>G
|
NP_001280160.1:p.Val83=
|
|
NM_001293233.1:c.*817C>G
|
NP_001280162.1:n.*817C>G
|
|
NM_005378.5:c.882C>G
|
NP_005369.2:p.Val294=
|
|
NM_005378.6:c.882C>G
MANE Select
|
NP_005369.2:p.Val294=
|
|
NM_001293228.2:c.882C>G
|
NP_001280157.1:p.Val294=
|
|
NM_001293231.2:c.249C>G
|
NP_001280160.1:p.Val83=
|
|
NM_001293233.2:c.*817C>G
|
NP_001280162.1:n.*817C>G
|
|