ENST00000703783.1:n.1048A>T
|
|
|
ENST00000703785.1:n.1129A>T
|
|
|
ENST00000262464.9:c.4264A>T
MANE Select
|
ENSP00000262464.4:p.Asn1422Tyr
|
|
ENST00000262464.8:c.4264A>T
|
ENSP00000262464.4:p.Asn1422Tyr
|
|
ENST00000507835.5:c.814A>T
|
ENSP00000426839.1:p.Asn272Tyr
|
|
ENST00000508053.5:c.4264A>T
|
ENSP00000424571.1:p.Asn1422Tyr
|
|
ENST00000508989.5:c.4165A>T
|
ENSP00000425596.1:p.Asn1389Tyr
|
|
ENST00000619499.4:c.4261A>T
|
ENSP00000482132.1:p.Asn1421Tyr
|
|
NM_001999.3:c.4264A>T
|
NP_001990.2:p.Asn1422Tyr
|
|
XM_017009228.2:c.4111A>T
|
XP_016864717.1:p.Asn1371Tyr
|
|
NM_001999.4:c.4264A>T
MANE Select
|
NP_001990.2:p.Asn1422Tyr
|
|