ENST00000703783.1:n.914A>C
|
|
|
ENST00000703785.1:n.995A>C
|
|
|
ENST00000262464.9:c.4130A>C
MANE Select
|
ENSP00000262464.4:p.Asn1377Thr
|
|
ENST00000262464.8:c.4130A>C
|
ENSP00000262464.4:p.Asn1377Thr
|
|
ENST00000507835.5:c.680A>C
|
ENSP00000426839.1:p.Asn227Thr
|
|
ENST00000508053.5:c.4130A>C
|
ENSP00000424571.1:p.Asn1377Thr
|
|
ENST00000508989.5:c.4031A>C
|
ENSP00000425596.1:p.Asn1344Thr
|
|
ENST00000619499.4:c.4127A>C
|
ENSP00000482132.1:p.Asn1376Thr
|
|
NM_001999.3:c.4130A>C
|
NP_001990.2:p.Asn1377Thr
|
|
XM_017009228.2:c.3977A>C
|
XP_016864717.1:p.Asn1326Thr
|
|
NM_001999.4:c.4130A>C
MANE Select
|
NP_001990.2:p.Asn1377Thr
|
|