ENST00000541682.7:c.358C>T
MANE Select
|
ENSP00000446205.2:p.Arg120Cys
|
|
ENST00000317814.8:c.343C>T
|
ENSP00000314774.4:p.Arg115Cys
|
|
ENST00000541682.6:c.358C>T
|
ENSP00000446205.2:p.Arg120Cys
|
|
ENST00000577735.1:c.334C>T
|
ENSP00000462491.1:p.Arg112Cys
|
|
NM_001165967.1:c.358C>T
|
NP_001159439.1:p.Arg120Cys
|
|
NM_032580.3:c.343C>T
|
NP_115969.2:p.Arg115Cys
|
|
XM_011524038.1:c.463C>T
|
XP_011522340.1:p.Arg155Cys
|
|
XM_011524039.1:c.454C>T
|
XP_011522341.1:p.Arg152Cys
|
|
XM_011524040.1:c.454C>T
|
XP_011522342.1:p.Arg152Cys
|
|
XM_011524041.1:c.445C>T
|
XP_011522343.1:p.Arg149Cys
|
|
XM_011524042.1:c.316C>T
|
XP_011522344.1:p.Arg106Cys
|
|
XR_934203.1:n.69+2092G>A
|
|
|
XM_017025232.1:c.463C>T
|
XP_016880721.1:p.Arg155Cys
|
|
XM_024451007.1:c.463C>T
|
XP_024306775.1:p.Arg155Cys
|
|
NM_001165967.2:c.358C>T
MANE Select
|
NP_001159439.1:p.Arg120Cys
|
|
NM_032580.4:c.343C>T
|
NP_115969.2:p.Arg115Cys
|
|