ENST00000399503.4:c.2902A>T
MANE Select
|
ENSP00000382423.3:p.Asn968Tyr
|
|
ENST00000399503.3:c.2902A>T
|
ENSP00000382423.3:p.Asn968Tyr
|
|
NM_005921.1:c.2902A>T
|
NP_005912.1:p.Asn968Tyr
|
|
XM_005248519.3:c.2524A>T
|
XP_005248576.2:p.Asn842Tyr
|
|
XM_011543406.1:c.2647A>T
|
XP_011541708.1:p.Asn883Tyr
|
|
XM_011543407.1:c.2623A>T
|
XP_011541709.1:p.Asn875Tyr
|
|
XM_011543408.1:c.2902A>T
|
XP_011541710.1:p.Asn968Tyr
|
|
XM_017009484.1:c.2491A>T
|
XP_016864973.1:p.Asn831Tyr
|
|
XM_017009485.1:c.2413A>T
|
XP_016864974.1:p.Asn805Tyr
|
|
XR_001742068.2:n.2933A>T
|
|
|
NM_005921.2:c.2902A>T
MANE Select
|
NP_005912.1:p.Asn968Tyr
|
|