ENST00000274008.5:c.556C>T
MANE Select
|
ENSP00000274008.3:p.Arg186Ter
|
|
ENST00000674886.1:n.618C>T
|
|
|
ENST00000675392.1:n.130C>T
|
|
|
ENST00000675612.1:c.553C>T
|
ENSP00000502453.1:p.Arg185Ter
|
|
ENST00000274008.4:c.556C>T
|
ENSP00000274008.3:p.Arg186Ter
|
|
ENST00000422835.2:n.598C>T
|
|
|
NM_145207.2:c.556C>T
|
NP_660208.2:p.Arg186Ter
|
|
XM_005262783.3:c.553C>T
|
XP_005262840.1:p.Arg185Ter
|
|
XM_011531678.1:c.553C>T
|
XP_011529980.1:p.Arg185Ter
|
|
XM_011531679.1:c.556C>T
|
XP_011529981.1:p.Arg186Ter
|
|
NM_001317799.1:c.553C>T
|
NP_001304728.1:p.Arg185Ter
|
|
NM_001345856.1:c.553C>T
|
NP_001332785.1:p.Arg185Ter
|
|
XM_011531678.2:c.553C>T
|
XP_011529980.1:p.Arg185Ter
|
|
XM_011531679.3:c.556C>T
|
XP_011529981.1:p.Arg186Ter
|
|
XM_017007825.1:c.556C>T
|
XP_016863314.1:p.Arg186Ter
|
|
XM_017007826.1:c.556C>T
|
XP_016863315.1:p.Arg186Ter
|
|
XM_017007827.2:c.556C>T
|
XP_016863316.1:p.Arg186Ter
|
|
XM_017007828.1:c.334C>T
|
XP_016863317.1:p.Arg112Ter
|
|
XM_017007829.1:c.100C>T
|
XP_016863318.1:p.Arg34Ter
|
|
XM_017007830.1:c.556C>T
|
XP_016863319.1:p.Arg186Ter
|
|
XR_001741151.1:n.626C>T
|
|
|
NM_145207.3:c.556C>T
MANE Select
|
NP_660208.2:p.Arg186Ter
|
|
NM_001317799.2:c.553C>T
|
NP_001304728.1:p.Arg185Ter
|
|
NM_001345856.2:c.553C>T
|
NP_001332785.1:p.Arg185Ter
|
|