ENST00000372548.9:c.1293T>C
MANE Select
|
ENSP00000361628.4:p.Asn431=
|
|
ENST00000372544.6:c.1293T>C
|
ENSP00000361623.2:p.Asn431=
|
|
ENST00000372548.8:c.1293T>C
|
ENSP00000361628.4:p.Asn431=
|
|
ENST00000421550.1:c.717T>C
|
ENSP00000405866.1:p.Asn239=
|
|
ENST00000461251.5:c.1293T>C
|
ENSP00000432238.1:p.Asn431=
|
|
NM_001184782.1:c.1293T>C
|
NP_001171711.1:p.Asn431=
|
|
NM_018015.5:c.1293T>C
|
NP_060485.4:p.Asn431=
|
|
XM_011530978.1:c.1293T>C
|
XP_011529280.1:p.Asn431=
|
|
XR_001755707.2:n.1417T>C
|
|
|
NM_018015.6:c.1293T>C
MANE Select
|
NP_060485.4:p.Asn431=
|
|
NM_001184782.2:c.1293T>C
|
NP_001171711.1:p.Asn431=
|
|