ENST00000211998.10:c.2875A>T
MANE Select
|
ENSP00000211998.5:p.Asn959Tyr
|
|
ENST00000211998.8:c.2875A>T
|
ENSP00000211998.4:p.Asn959Tyr
|
|
ENST00000372755.7:c.2746-2146A>T
|
ENSP00000361841.3:n.2746-2146A>T
|
|
ENST00000436396.1:c.1891A>T
|
ENSP00000415489.1:p.Asn631Tyr
|
|
ENST00000623461.3:n.5549-2146A>T
|
|
|
ENST00000624354.3:c.*2630A>T
|
ENSP00000485551.1:n.*2630A>T
|
|
NM_003373.3:c.2746-2146A>T
|
NP_003364.1:n.2746-2146A>T
|
|
NM_014000.2:c.2875A>T , LRG_383t1:c.2875A>T
|
NP_054706.1:p.Asn959Tyr
|
|
XM_005270142.1:c.2878A>T
|
XP_005270199.1:p.Asn960Tyr
|
|
XM_005270143.1:c.2749-2146A>T
|
XP_005270200.1:n.2749-2146A>T
|
|
NM_003373.4:c.2746-2146A>T
|
NP_003364.1:n.2746-2146A>T
|
|
NM_014000.3:c.2875A>T
MANE Select
|
NP_054706.1:p.Asn959Tyr
|
|