ENST00000274008.5:c.1615A>T
MANE Select
|
ENSP00000274008.3:p.Arg539Trp
|
|
ENST00000674886.1:n.1677A>T
|
|
|
ENST00000675612.1:c.1612A>T
|
ENSP00000502453.1:p.Arg538Trp
|
|
ENST00000274008.4:c.1615A>T
|
ENSP00000274008.3:p.Arg539Trp
|
|
ENST00000422835.2:n.1657A>T
|
|
|
NM_145207.2:c.1615A>T
|
NP_660208.2:p.Arg539Trp
|
|
XM_005262783.3:c.1612A>T
|
XP_005262840.1:p.Arg538Trp
|
|
XM_011531678.1:c.1612A>T
|
XP_011529980.1:p.Arg538Trp
|
|
XM_011531679.1:c.1615A>T
|
XP_011529981.1:p.Arg539Trp
|
|
NM_001317799.1:c.1612A>T
|
NP_001304728.1:p.Arg538Trp
|
|
NM_001345856.1:c.1612A>T
|
NP_001332785.1:p.Arg538Trp
|
|
XM_011531678.2:c.1612A>T
|
XP_011529980.1:p.Arg538Trp
|
|
XM_011531679.3:c.1615A>T
|
XP_011529981.1:p.Arg539Trp
|
|
XM_017007825.1:c.1615A>T
|
XP_016863314.1:p.Arg539Trp
|
|
XM_017007826.1:c.1615A>T
|
XP_016863315.1:p.Arg539Trp
|
|
XM_017007827.2:c.1615A>T
|
XP_016863316.1:p.Arg539Trp
|
|
XM_017007828.1:c.1393A>T
|
XP_016863317.1:p.Arg465Trp
|
|
XM_017007829.1:c.1159A>T
|
XP_016863318.1:p.Arg387Trp
|
|
XM_017007830.1:c.1615A>T
|
XP_016863319.1:p.Arg539Trp
|
|
XR_001741151.1:n.1685A>T
|
|
|
NM_145207.3:c.1615A>T
MANE Select
|
NP_660208.2:p.Arg539Trp
|
|
NM_001317799.2:c.1612A>T
|
NP_001304728.1:p.Arg538Trp
|
|
NM_001345856.2:c.1612A>T
|
NP_001332785.1:p.Arg538Trp
|
|