ENST00000394308.8:c.1257A>C
MANE Select
|
ENSP00000377845.3:p.Pro419=
|
|
ENST00000175506.8:c.1257A>C
|
ENSP00000175506.4:p.Pro419=
|
|
ENST00000394308.7:c.1257A>C
|
ENSP00000377845.3:p.Pro419=
|
|
ENST00000394309.7:c.1257A>C
|
ENSP00000377846.3:p.Pro419=
|
|
ENST00000422745.5:c.1194A>C
|
ENSP00000414901.1:p.Pro398=
|
|
ENST00000437628.5:c.1008A>C
|
ENSP00000414379.1:p.Pro336=
|
|
ENST00000444334.5:c.1194A>C
|
ENSP00000406994.1:p.Pro398=
|
|
ENST00000454046.5:c.*125A>C
|
ENSP00000401651.1:n.*125A>C
|
|
ENST00000455086.5:c.1008A>C
|
ENSP00000408472.1:p.Pro336=
|
|
ENST00000487714.1:n.315A>C
|
|
|
NM_001178075.1:c.1194A>C
|
NP_001171546.1:p.Pro398=
|
|
NM_001178076.1:c.1008A>C
|
NP_001171547.1:p.Pro336=
|
|
NM_001178077.1:c.1008A>C
|
NP_001171548.1:p.Pro336=
|
|
NM_001673.4:c.1257A>C
|
NP_001664.3:p.Pro419=
|
|
NM_133436.3:c.1257A>C
|
NP_597680.2:p.Pro419=
|
|
NM_183356.3:c.1257A>C
|
NP_899199.2:p.Pro419=
|
|
NM_001352496.1:c.1257A>C
|
NP_001339425.1:p.Pro419=
|
|
NR_147989.1:n.2960A>C
|
|
|
NM_001673.5:c.1257A>C
MANE Select
|
NP_001664.3:p.Pro419=
|
|
NM_001178075.2:c.1194A>C
|
NP_001171546.1:p.Pro398=
|
|
NM_001178076.2:c.1008A>C
|
NP_001171547.1:p.Pro336=
|
|
NM_001352496.2:c.1257A>C
|
NP_001339425.1:p.Pro419=
|
|
NM_183356.4:c.1257A>C
|
NP_899199.2:p.Pro419=
|
|