ENST00000298139.7:c.3506A>C
MANE Select
|
ENSP00000298139.5:p.Asn1169Thr
|
|
ENST00000650667.1:c.*3120A>C
|
ENSP00000498593.1:n.*3120A>C
|
|
ENST00000298139.5:c.3506A>C
|
ENSP00000298139.5:p.Asn1169Thr
|
|
ENST00000521620.5:n.2139A>C
|
|
|
NM_000553.4:c.3506A>C , LRG_524t1:c.3506A>C
|
NP_000544.2:p.Asn1169Thr
|
|
XM_011544639.1:c.3425A>C
|
XP_011542941.1:p.Asn1142Thr
|
|
XM_011544640.1:c.1907A>C
|
XP_011542942.1:p.Asn636Thr
|
|
XR_949470.1:n.3779A>C
|
|
|
XR_949471.1:n.3779A>C
|
|
|
XR_949472.1:n.3779A>C
|
|
|
XR_949643.1:n.614+1098T>G
|
|
|
NM_000553.5:c.3506A>C
|
NP_000544.2:p.Asn1169Thr
|
|
XM_011544639.3:c.3425A>C
|
XP_011542941.1:p.Asn1142Thr
|
|
XM_024447265.1:c.3296A>C
|
XP_024303033.1:p.Asn1099Thr
|
|
XR_949470.3:n.3807A>C
|
|
|
XR_949471.3:n.3807A>C
|
|
|
XR_949472.3:n.3807A>C
|
|
|
NM_000553.6:c.3506A>C
MANE Select
|
NP_000544.2:p.Asn1169Thr
|
|