ENST00000541682.7:c.278T>A
MANE Select
|
ENSP00000446205.2:p.Leu93His
|
|
ENST00000317814.8:c.263T>A
|
ENSP00000314774.4:p.Leu88His
|
|
ENST00000541682.6:c.278T>A
|
ENSP00000446205.2:p.Leu93His
|
|
ENST00000577735.1:c.254T>A
|
ENSP00000462491.1:p.Leu85His
|
|
NM_001165967.1:c.278T>A
|
NP_001159439.1:p.Leu93His
|
|
NM_032580.3:c.263T>A
|
NP_115969.2:p.Leu88His
|
|
XM_011524038.1:c.383T>A
|
XP_011522340.1:p.Leu128His
|
|
XM_011524039.1:c.374T>A
|
XP_011522341.1:p.Leu125His
|
|
XM_011524040.1:c.374T>A
|
XP_011522342.1:p.Leu125His
|
|
XM_011524041.1:c.365T>A
|
XP_011522343.1:p.Leu122His
|
|
XM_011524042.1:c.236T>A
|
XP_011522344.1:p.Leu79His
|
|
XR_934203.1:n.69+2172A>T
|
|
|
XM_017025232.1:c.383T>A
|
XP_016880721.1:p.Leu128His
|
|
XM_024451007.1:c.383T>A
|
XP_024306775.1:p.Leu128His
|
|
NM_001165967.2:c.278T>A
MANE Select
|
NP_001159439.1:p.Leu93His
|
|
NM_032580.4:c.263T>A
|
NP_115969.2:p.Leu88His
|
|