ENST00000392492.8:c.272T>A
MANE Select
|
ENSP00000376282.2:p.Val91Glu
|
|
ENST00000250615.7:c.407T>A
|
ENSP00000250615.2:p.Val136Glu
|
|
ENST00000392492.7:c.272T>A
|
ENSP00000376282.2:p.Val91Glu
|
|
ENST00000585649.1:c.386T>A
|
ENSP00000468717.1:p.Val129Glu
|
|
ENST00000587798.1:c.*49T>A
|
ENSP00000468239.1:n.*49T>A
|
|
NM_001088.2:c.272T>A
|
NP_001079.1:p.Val91Glu
|
|
NM_001166579.1:c.407T>A
|
NP_001160051.1:p.Val136Glu
|
|
NR_110548.1:n.583T>A
|
|
|
XM_011524415.1:c.272T>A
|
XP_011522717.1:p.Val91Glu
|
|
XM_011524416.1:c.479T>A
|
XP_011522718.1:p.Val160Glu
|
|
XM_011524417.1:c.479T>A
|
XP_011522719.1:p.Val160Glu
|
|
XM_011524418.1:c.479T>A
|
XP_011522720.1:p.Val160Glu
|
|
XM_011524419.1:c.479T>A
|
XP_011522721.1:p.Val160Glu
|
|
XM_011524420.1:c.479T>A
|
XP_011522722.1:p.Val160Glu
|
|
XM_011524421.1:c.479T>A
|
XP_011522723.1:p.Val160Glu
|
|
XM_011524422.1:c.362T>A
|
XP_011522724.1:p.Val121Glu
|
|
XM_011524423.1:c.272T>A
|
XP_011522725.1:p.Val91Glu
|
|
XM_017024259.1:c.386T>A
|
XP_016879748.1:p.Val129Glu
|
|
NM_001088.3:c.272T>A
MANE Select
|
NP_001079.1:p.Val91Glu
|
|
NR_110548.2:n.528T>A
|
|
|
NM_001166579.2:c.407T>A
|
NP_001160051.1:p.Val136Glu
|
|