ENST00000541682.7:c.477T>A
MANE Select
|
ENSP00000446205.2:p.Leu159=
|
|
ENST00000317814.8:c.462T>A
|
ENSP00000314774.4:p.Leu154=
|
|
ENST00000541682.6:c.477T>A
|
ENSP00000446205.2:p.Leu159=
|
|
NM_001165967.1:c.477T>A
|
NP_001159439.1:p.Leu159=
|
|
NM_032580.3:c.462T>A
|
NP_115969.2:p.Leu154=
|
|
XM_011524038.1:c.582T>A
|
XP_011522340.1:p.Leu194=
|
|
XM_011524039.1:c.573T>A
|
XP_011522341.1:p.Leu191=
|
|
XM_011524040.1:c.573T>A
|
XP_011522342.1:p.Leu191=
|
|
XM_011524041.1:c.564T>A
|
XP_011522343.1:p.Leu188=
|
|
XM_011524042.1:c.435T>A
|
XP_011522344.1:p.Leu145=
|
|
XR_934203.1:n.69+1973A>T
|
|
|
XM_017025232.1:c.582T>A
|
XP_016880721.1:p.Leu194=
|
|
XM_024451007.1:c.582T>A
|
XP_024306775.1:p.Leu194=
|
|
NM_001165967.2:c.477T>A
MANE Select
|
NP_001159439.1:p.Leu159=
|
|
NM_032580.4:c.462T>A
|
NP_115969.2:p.Leu154=
|
|