ENST00000397545.9:c.2729G>C
MANE Select
|
ENSP00000380679.4:p.Trp910Ser
|
|
ENST00000374877.7:c.2729G>C
|
ENSP00000364011.3:p.Trp910Ser
|
|
ENST00000397545.8:c.2729G>C
|
ENSP00000380679.4:p.Trp910Ser
|
|
ENST00000572253.5:n.2980G>C
|
|
|
ENST00000573903.1:n.391G>C
|
|
|
ENST00000574799.5:n.2266G>C
|
|
|
ENST00000575431.1:n.373G>C
|
|
|
NM_001243342.1:c.2729G>C
|
NP_001230271.1:p.Trp910Ser
|
|
NM_017950.3:c.2729G>C
|
NP_060420.2:p.Trp910Ser
|
|
XM_011524963.1:c.2639G>C
|
XP_011523265.1:p.Trp880Ser
|
|
XM_011524964.1:c.1550G>C
|
XP_011523266.1:p.Trp517Ser
|
|
XR_934495.1:n.2847G>C
|
|
|
XM_011524963.3:c.2639G>C
|
XP_011523265.1:p.Trp880Ser
|
|
XM_011524964.3:c.1550G>C
|
XP_011523266.1:p.Trp517Ser
|
|
XM_024450821.1:c.2639G>C
|
XP_024306589.1:p.Trp880Ser
|
|
XR_934495.2:n.2847G>C
|
|
|
NM_017950.4:c.2729G>C
MANE Select
|
NP_060420.2:p.Trp910Ser
|
|
NM_001243342.2:c.2729G>C
|
NP_001230271.1:p.Trp910Ser
|
|