ENST00000368666.7:c.1003T>A
MANE Select
|
ENSP00000357655.4:p.Cys335Ser
|
|
ENST00000639360.1:c.904T>A
|
ENSP00000491774.1:p.Cys302Ser
|
|
ENST00000230529.9:c.1003T>A
|
ENSP00000230529.5:p.Cys335Ser
|
|
ENST00000361714.5:c.1003T>A
|
ENSP00000354734.2:p.Cys335Ser
|
|
ENST00000368663.4:c.*309T>A
|
ENSP00000357652.4:n.*309T>A
|
|
ENST00000368664.7:c.*407T>A
|
ENSP00000357653.3:n.*407T>A
|
|
ENST00000368666.6:c.1057T>A
|
ENSP00000357655.3:p.Cys353Ser
|
|
ENST00000409166.5:c.331T>A
|
ENSP00000386467.1:p.Cys111Ser
|
|
ENST00000454589.5:c.*407T>A
|
ENSP00000395928.1:n.*407T>A
|
|
ENST00000604763.5:c.1003T>A
|
ENSP00000473777.1:p.Cys335Ser
|
|
ENST00000613648.1:n.838T>A
|
|
|
ENST00000620524.3:n.934T>A
|
|
|
NM_003880.3:c.1003T>A
|
NP_003871.1:p.Cys335Ser
|
|
NM_198239.1:c.1057T>A
|
NP_937882.1:p.Cys353Ser
|
|
NR_125353.1:n.1257T>A
|
|
|
NR_125354.1:n.1177T>A
|
|
|
XM_011536220.1:c.1003T>A
|
XP_011534522.1:p.Cys335Ser
|
|
XM_011536221.1:c.*407T>A
|
XP_011534523.1:n.*407T>A
|
|
XM_011536223.1:c.421T>A
|
XP_011534525.1:p.Cys141Ser
|
|
XM_011536223.3:c.421T>A
|
XP_011534525.1:p.Cys141Ser
|
|
XR_001743705.1:n.1605T>A
|
|
|
NM_003880.4:c.1003T>A
|
NP_003871.1:p.Cys335Ser
|
|
NM_198239.2:c.1003T>A
MANE Select
|
NP_937882.2:p.Cys335Ser
|
|
NR_125353.2:n.1321T>A
|
|
|
NR_125354.3:n.1148T>A
|
|
|