ENST00000397545.9:c.2714A>G
MANE Select
|
ENSP00000380679.4:p.His905Arg
|
|
ENST00000374877.7:c.2714A>G
|
ENSP00000364011.3:p.His905Arg
|
|
ENST00000397545.8:c.2714A>G
|
ENSP00000380679.4:p.His905Arg
|
|
ENST00000572253.5:n.2965A>G
|
|
|
ENST00000573903.1:n.376A>G
|
|
|
ENST00000574799.5:n.2251A>G
|
|
|
ENST00000575431.1:n.358A>G
|
|
|
NM_001243342.1:c.2714A>G
|
NP_001230271.1:p.His905Arg
|
|
NM_017950.3:c.2714A>G
|
NP_060420.2:p.His905Arg
|
|
XM_011524963.1:c.2624A>G
|
XP_011523265.1:p.His875Arg
|
|
XM_011524964.1:c.1535A>G
|
XP_011523266.1:p.His512Arg
|
|
XR_934495.1:n.2832A>G
|
|
|
XM_011524963.3:c.2624A>G
|
XP_011523265.1:p.His875Arg
|
|
XM_011524964.3:c.1535A>G
|
XP_011523266.1:p.His512Arg
|
|
XM_024450821.1:c.2624A>G
|
XP_024306589.1:p.His875Arg
|
|
XR_934495.2:n.2832A>G
|
|
|
NM_017950.4:c.2714A>G
MANE Select
|
NP_060420.2:p.His905Arg
|
|
NM_001243342.2:c.2714A>G
|
NP_001230271.1:p.His905Arg
|
|