NM_003734.4:c.805C>T
MANE Select
|
NP_003725.1:p.Arg269Cys
|
ENST00000308423.7:c.805C>T
MANE Select
|
ENSP00000312326.1:p.Arg269Cys
|
NM_001277731.1:c.805C>T
|
NP_001264660.1:p.Arg269Cys
|
NM_001277731.2:c.805C>T
|
NP_001264660.1:p.Arg269Cys
|
NM_003734.3:c.805C>T
|
NP_003725.1:p.Arg269Cys
|
NR_102422.1:n.965C>T
|
|
NR_102422.2:n.950C>T
|
|
ENST00000308423.6:c.805C>T
|
ENSP00000312326.1:p.Arg269Cys
|
ENST00000613571.1:c.805C>T
|
ENSP00000484312.1:p.Arg269Cys
|
XM_011525419.1:c.805C>T
|
XP_011523721.1:p.Arg269Cys
|
XM_011525419.2:c.805C>T
|
XP_011523721.1:p.Arg269Cys
|
XM_011525420.1:c.805C>T
|
XP_011523722.1:p.Arg269Cys
|
XM_011525420.3:c.805C>T
|
XP_011523722.1:p.Arg269Cys
|
XR_001752673.2:n.967C>T
|
|
XR_934584.1:n.1026C>T
|
|
XR_934584.2:n.967C>T
|
|