ENST00000703783.1:n.649A>T
|
|
|
ENST00000703785.1:n.730A>T
|
|
|
ENST00000262464.9:c.3865A>T
MANE Select
|
ENSP00000262464.4:p.Asn1289Tyr
|
|
ENST00000262464.8:c.3865A>T
|
ENSP00000262464.4:p.Asn1289Tyr
|
|
ENST00000507835.5:c.415A>T
|
ENSP00000426839.1:p.Asn139Tyr
|
|
ENST00000508053.5:c.3865A>T
|
ENSP00000424571.1:p.Asn1289Tyr
|
|
ENST00000508989.5:c.3766A>T
|
ENSP00000425596.1:p.Asn1256Tyr
|
|
ENST00000619499.4:c.3862A>T
|
ENSP00000482132.1:p.Asn1288Tyr
|
|
NM_001999.3:c.3865A>T
|
NP_001990.2:p.Asn1289Tyr
|
|
XM_017009228.2:c.3712A>T
|
XP_016864717.1:p.Asn1238Tyr
|
|
NM_001999.4:c.3865A>T
MANE Select
|
NP_001990.2:p.Asn1289Tyr
|
|