ENST00000537228.6:c.441A>T
|
ENSP00000445691.1:p.Arg147Ser
|
|
ENST00000543081.6:c.427+336A>T
|
ENSP00000439103.2:n.427+336A>T
|
|
ENST00000544516.6:c.157-542A>T
|
ENSP00000439538.2:n.157-542A>T
|
|
ENST00000545576.2:n.872A>T
|
|
|
ENST00000696246.1:c.426A>T
|
ENSP00000512504.1:p.Arg142Ser
|
|
ENST00000696271.1:n.883A>T
|
|
|
ENST00000696272.1:c.456A>T
|
ENSP00000512515.1:p.Arg152Ser
|
|
ENST00000696273.1:c.504A>T
|
ENSP00000512516.1:p.Arg168Ser
|
|
ENST00000229335.11:c.471A>T
MANE Select
|
ENSP00000229335.6:p.Arg157Ser
|
|
ENST00000229335.10:c.471A>T
|
ENSP00000229335.6:p.Arg157Ser
|
|
ENST00000537228.5:c.441A>T
|
ENSP00000445691.1:p.Arg147Ser
|
|
ENST00000543081.5:c.423+336A>T
|
|
|
ENST00000544516.5:c.153-542A>T
|
|
|
ENST00000545512.1:c.467A>T
|
|
|
ENST00000545576.1:n.797A>T
|
|
|
NM_020661.2:c.471A>T , LRG_17t1:c.471A>T
|
NP_065712.1:p.Arg157Ser
|
|
XM_011520772.1:c.441A>T
|
XP_011519074.1:p.Arg147Ser
|
|
XM_011520773.1:c.427+336A>T
|
XP_011519075.1:n.427+336A>T
|
|
NM_001330343.1:c.441A>T
|
NP_001317272.1:p.Arg147Ser
|
|
NM_020661.3:c.471A>T
|
NP_065712.1:p.Arg157Ser
|
|
XM_011520773.2:c.427+336A>T
|
XP_011519075.1:n.427+336A>T
|
|
NM_020661.4:c.471A>T
MANE Select
|
NP_065712.1:p.Arg157Ser
|
|
NM_001330343.2:c.441A>T
|
NP_001317272.1:p.Arg147Ser
|
|