ENST00000399503.4:c.2557C>T
MANE Select
|
ENSP00000382423.3:p.Arg853Cys
|
|
ENST00000399503.3:c.2557C>T
|
ENSP00000382423.3:p.Arg853Cys
|
|
NM_005921.1:c.2557C>T
|
NP_005912.1:p.Arg853Cys
|
|
XM_005248519.3:c.2179C>T
|
XP_005248576.2:p.Arg727Cys
|
|
XM_011543406.1:c.2302C>T
|
XP_011541708.1:p.Arg768Cys
|
|
XM_011543407.1:c.2278C>T
|
XP_011541709.1:p.Arg760Cys
|
|
XM_011543408.1:c.2557C>T
|
XP_011541710.1:p.Arg853Cys
|
|
XM_017009484.1:c.2146C>T
|
XP_016864973.1:p.Arg716Cys
|
|
XM_017009485.1:c.2068C>T
|
XP_016864974.1:p.Arg690Cys
|
|
XR_001742068.2:n.2588C>T
|
|
|
NM_005921.2:c.2557C>T
MANE Select
|
NP_005912.1:p.Arg853Cys
|
|