ENST00000703162.1:n.238T>G
|
|
|
ENST00000281043.4:c.889T>G
MANE Select
|
ENSP00000281043.3:p.Phe297Val
|
|
ENST00000638417.1:c.256T>G
|
ENSP00000491476.1:p.Phe86Val
|
|
ENST00000281043.3:c.889T>G
|
ENSP00000281043.3:p.Phe297Val
|
|
NM_001293228.1:c.889T>G
|
NP_001280157.1:p.Phe297Val
|
|
NM_001293231.1:c.256T>G
|
NP_001280160.1:p.Phe86Val
|
|
NM_001293233.1:c.*824T>G
|
NP_001280162.1:n.*824T>G
|
|
NM_005378.5:c.889T>G
|
NP_005369.2:p.Phe297Val
|
|
NM_005378.6:c.889T>G
MANE Select
|
NP_005369.2:p.Phe297Val
|
|
NM_001293228.2:c.889T>G
|
NP_001280157.1:p.Phe297Val
|
|
NM_001293231.2:c.256T>G
|
NP_001280160.1:p.Phe86Val
|
|
NM_001293233.2:c.*824T>G
|
NP_001280162.1:n.*824T>G
|
|