ENST00000703783.1:n.311A>C
|
|
|
ENST00000703785.1:n.392A>C
|
|
|
ENST00000262464.9:c.3527A>C
MANE Select
|
ENSP00000262464.4:p.Asn1176Thr
|
|
ENST00000262464.8:c.3527A>C
|
ENSP00000262464.4:p.Asn1176Thr
|
|
ENST00000507835.5:c.77A>C
|
ENSP00000426839.1:p.Asn26Thr
|
|
ENST00000508053.5:c.3527A>C
|
ENSP00000424571.1:p.Asn1176Thr
|
|
ENST00000508989.5:c.3428A>C
|
ENSP00000425596.1:p.Asn1143Thr
|
|
ENST00000619499.4:c.3524A>C
|
ENSP00000482132.1:p.Asn1175Thr
|
|
NM_001999.3:c.3527A>C
|
NP_001990.2:p.Asn1176Thr
|
|
XM_017009228.2:c.3374A>C
|
XP_016864717.1:p.Asn1125Thr
|
|
NM_001999.4:c.3527A>C
MANE Select
|
NP_001990.2:p.Asn1176Thr
|
|